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5,6-Dihydro-6-hydroxy-5,5-dimethyl-7-(2-oxopyrrolidin-1-yl)-7H-thieno[3,2-b]pyran

中文名称
——
中文别名
——
英文名称
5,6-Dihydro-6-hydroxy-5,5-dimethyl-7-(2-oxopyrrolidin-1-yl)-7H-thieno[3,2-b]pyran
英文别名
1-(6-hydroxy-5,5-dimethyl-6,7-dihydrothieno[3,2-b]pyran-7-yl)pyrrolidin-2-one
5,6-Dihydro-6-hydroxy-5,5-dimethyl-7-(2-oxopyrrolidin-1-yl)-7H-thieno[3,2-b]pyran化学式
CAS
——
化学式
C13H17NO3S
mdl
——
分子量
267.35
InChiKey
YVDVXXLNFSKUSO-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.8
  • 重原子数:
    18
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    78
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

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文献信息

  • Substituted thienopyrans as antihypertensive agents
    申请人:Ortho Pharmaceutical Corporation
    公开号:US04992435A1
    公开(公告)日:1991-02-12
    Substituted thienopyrans and processes for preparing the thienopyrans are disclosed. The thienopyrans are useful as antihypertensive agents; antianginals are peripheral antivasoconstrictive agents.
    本文介绍了替代噻吩并制备噻吩衍生物的过程。这些噻吩衍生物可用作降压剂、抗心绞痛剂和外周抗血管收缩剂。
  • Substituted thienopyrans
    申请人:Ortho Pharmaceutical Corporation
    公开号:US05030736A1
    公开(公告)日:1991-07-09
    Substituted thienopyrans and processes for preparing the thienopyrans are disclosed. The thienopyrans are useful as antihypertensive agents; antianginals are peripheral antivasoconstrictive agents.
    本发明揭示了替代噻吩并制备噻吩的过程。这些噻吩可用作降压剂;抗心绞痛和外周抗血管收缩剂。
  • The process for the preparation of enantiomerically pure thienopyran derivative
    申请人:ORTHO PHARMACEUTICAL CORPORATION
    公开号:EP0493048A1
    公开(公告)日:1992-07-01
    A process for the preparation of enantiomerically pure thienopyran derivatives of the formula is described. The thienopyran derivatives are relaxants of smooth muscle tone and as such are useful in vascular tissue for the treatment of hypertension disease, angina and other vascular disorders characterized by poor regional perfusion.
    一种制备对映体纯的式噻吩并吡喃衍生物的工艺 的对映体纯噻喃衍生物的制备方法。噻喃衍生物是平滑肌张力的松弛剂,因此可用于血管组织,治疗高血压病、心绞痛和其他以区域灌注不良为特征的血管疾病。
  • [DE] ORTHO-SUBSTITUIERTE 2-METHOXYIMINOPHENYLESSIGSÄUREMETHYLAMIDE<br/>[EN] ORTHO-SUBSTITUTED 2-METHOXYIMINOPHENYLACETIC ACID METHYLAMIDES<br/>[FR] METHYLAMIDES DE L'ACIDE 2-METHOXYIMINOPHENYLACETIQUE ORTHO-SUBSTITUES
    申请人:BASF AKTIENGESELLSCHAFT
    公开号:WO1994019331A1
    公开(公告)日:1994-09-01
    (DE) Verbindungen der allgemeinen Formel (I) in der der Index und die Substituenten die folgende Bedeutung haben: n 0, 1 bis 4; X O oder S; Y ein fünfringheteroaromatischer Ring; R1 Nitro; Cyano; Halogen; Alkyl; Halogenalkyl; Alkoxy; Halogenalkoxy; Alkylthio; Phenyl oder Phenoxy; R2 Wasserstoff; Alkyl, Alkenyl oder Alkinyl; ein gesättigter oder ungesättigter Ring, welcher neben Kohlenstoffatomen noch Heteroatome als ringglieder enthalten kann.(EN) The invention concerns compounds of formula (I) in which the subscript and the substituents are defined as: n is 0 or 1 to 4; X is 0 or S; Y is a five-membered aromatic heterocycle ring; R1 is nitro, cyano, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, phenyl or phenoxy; R2 is hydrogen, alkyl, alkenyl, alkinyl or a saturated or unsaturated ring which may include heteroatoms in addition to carbon atoms as ring members.(FR) Composés de formule générale (I) dans laquelle l'indice et les substituants ont les notations: N = 0, 1 à 4; X = O ou S; Y désigne un cycle hétéroaromatique à noyau pentagonal; R1 est nitro, cyano, halogène; alkyle, halogénoalkyle, alkoxy, halogénoalkoxy, alkylthio; phényle ou phénoxy; R2 est hydrogène, alkyle, alcényle ou alcinyle; un noyau saturé ou insaturé pouvant renfermer, en plus d'atomes de carbone, des hétéro-atomes comme chaînons du cycle.
    (DE) 化合物的通用式(I)中,下标和取代基团具有如下意义:n为0或1至4;X为O或S;Y为五个成员的芳香杂环;R1为硝基、CN基、卤素、烷基、卤化烷基、醚基、卤化醚基、硫化烷基、苯基或邻苯基;R2为氢、烷基、烯基或炔基,或者是饱和或不饱和的环,即使环中含有除碳原子外的其他元素。 (EN) The compounds have the general formula (I) wherein the index and substituents are defined as: n is 0 or 1 to 4; X is O or S; Y is a five-membered aromatic heterocycle; R1 is nitro, cyano, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, phenyl or phenoxy; R2 is hydrogen, alkyl, alkenyl or alkinyl or a saturated or unsaturated ring containing heteroatoms in addition to carbon atoms. (_FR) Les composés suivent la formule générale (I) où le đièdre et les substituents sont définis comme suit : n = 0 ou 1 à 4 ; X = O ou S ; Y désigne un cycle hétéroaromatique à noyau pentagonal ; R1 est nitro, cyano, halogène ; alkyle, haloalkyle, alkoxy, haloalkoxy, alkylthio ; phényle ou phénoxy ; R2 est hydrogène, alkyle, alcényle ou alcinyle ; un noyau saturé ou insaturé pouvant renfermer, outre les atomes de carbone, des hétéroatomes commeChaîns du cycle.
  • ORTHO-SUBSTITUIERTE 2-METHOXYIMINOPHENYLESSIGSÄUREMETHYLAMIDE
    申请人:BASF Aktiengesellschaft
    公开号:EP0686152A1
    公开(公告)日:1995-12-13
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同类化合物

化合物SEP-363856HYDROCHLORIDE 6,7-二氢-4H-噻吩并[3,2-c]吡喃-4-甲胺 6,7-二氢-4H-噻吩并[3,2-c]吡喃-2-羧酸乙酯 6,7-二氢-4H-噻吩并[3,2-c]吡喃-2-羧酸 5,7-二氢-4H-噻吩并[2,3-c]吡喃-3-羧酸 5,7-二氢-4H-噻吩并[2,3-C]吡喃-3-羧酸乙酯 4-(2-羟基乙基)-4-甲基-6,7-二氢-4h-噻吩并[3,2-c]吡喃 4,5-二氢螺[哌啶-4,7-噻吩并[2,3-c]吡喃] 4',5'-二氢-螺[哌啶-4,7'-[7H]噻吩并[2,3-c]吡喃]-1-羧酸叔丁酯 2-氯-4,5-二氢螺[哌啶-4,7-噻吩并[2,3-c]吡喃] 2-氨基-5,5-二甲基-4,7-二氢-5H-噻吩并[2,3-C]吡喃-3-羧酸叔丁酯 2-氨基-4,7-二氢-5H-噻吩并[2,3-c]吡喃-3-羧酸乙酯 2-氨基-4,7-二氢-5H-噻吩并[2,3-c]吡喃-3-甲腈 2-[[(苯甲酰基氨基)硫代甲酰]氨基]-4,7-二氢-5,5-二甲基-5H-噻吩并[2,3-C]吡喃-3-羧酸 (4-甲基-6,7-二氢-4H-噻吩并[3,2-c]吡喃-4-基)乙酸 (2-羧基噻吩-3-基)乙酸酐 2-(3-hydroxy-2,2-dimethylpropanamido)-5,5,7,7-tetramethyl-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxamide 2-[[(2S)-2-hydroxy-3,3-dimethylbutanoyl]amino]-5,5,7,7-tetramethyl-4H-thieno[2,3-c]pyran-3-carboxamide N-(3-carbamoyl-5,5,7,7-tetramethyl-5,7-dihydro-4H-thieno[2,3-c]pyran-2-yl)-4-chloro-5-methyl-1H-pyrazole-3-carboxamide N-(3-carbamoyl-5,5,7,7-tetramethyl-5,7-dihydro-4H-thieno[2,3-c]pyran-2-yl)-2-fluoronicotinamide N-(3-carbamoyl-5,5,7,7-tetramethyl-5,7-dihydro-4H-thieno[2,3-c]pyran-2-yl)-2-oxopyrrolidine-3-carboxamide 2-(1-(hydroxymethyl)cyclopropanecarboxamido)-5,5,7,7-tetramethyl-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxamide N-(3-carbamoyl-5,5,7,7-tetramethyl-5,7-dihydro-4H-thieno[2,3-c]pyran-2-yl)-1H-pyrazole-5-carboxamide tert-butyl 2-(3-(3,4-dimethoxyphenyl)thioureido)-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxylate trans-6-(benzyloxy)-2-carbamoyl-5,6-dihydro-5,5-dimethyl-7-(2-oxopiperidin-1-yl)-5H-thieno<3,2-b>pyran trans-6-(benzyloxy)-2-carbomethoxy-5,6-dihydro-5,5-dimethyl-7-(2-oxopiperidin-1-yl)-5H-thieno<3,2-b>pyran trans-6-(benzyloxy)-2-cyano-5,6-dihydro-5,5-dimethyl-7-(2-oxopiperidin-1-yl)-5H-thieno<3,2-b>pyran trans-5,6-dihydro-6-hydroxy-5,5-dimethyl-7-(2-oxopiperidin-1-yl)-5H-thieno<3,2-b>pyran trans-6-(benzyloxy)-2-bromo-5,6-dihydro-5,5-dimethyl-7-(2-oxopiperidin-1-yl)-5H-thieno<3,2-b>pyran trans-2-bromo-5,6-dihydro-6-hydroxy-5,5-dimethyl-7-(2-oxopiperidin-1-yl)-5H-thieno<3,2-b>pyran (-)-trans-5,6-dihydro-6-hydroxy-5,5-dimethyl-7-(2-oxopiperidin-1-yl)-5H-thieno<3,2-b>pyran 5,5-dimethyl-2-nitro-7-(2-oxopiperidin-1-yl)-5H-thieno<3,2-b>pyran trans-2-cyano-5,6-dihydro-6-hydroxy-5,5-dimethyl-7-(2-oxopiperidin-1-yl)-5H-thieno<3,2-b>pyran (-)-trans-5,6-dihydro-6-hydroxy-5,5-dimethyl-2-nitro-7-(2-oxopiperidin-1-yl)-5H-thieno<3,2-b>pyran trans-5,6-dihydro-6-hydroxy-5,5-dimethyl-2-nitro-7-(2-oxopiperidin-1-yl)-5H-thieno<3,2-b>pyran cis-7-amino-5,6-dihydro-6-hydroxy-5,5-dimethyl-5H-thieno<3,2-b>pyran 2-[3-(3-trifluoromethyl[1,2,4]oxadiazol-5-yl)-4,7-dihydro-5H-thieno[2,3-c]pyran-2-ylcarbamoyl]cyclopent-1-enecarboxylic acid 2-[3-(4-trifluoromethylthiazol-2-yl)-4,7-dihydro-5H-thieno[2,3-c]pyran-2-ylcarbamoyl]cyclopent-1-enecarboxylic acid 2-[3-(4,5-dimethyloxazol-2-yl)-4,7-dihydro-5H-thieno[2,3-c]pyran-2-ylcarbamoyl]cyclopent-1-enecarboxylic acid 4,4-dimethyl-6,7-dihydro-4H-thieno[3,2-c]pyran 1,1-(3-dimethylamino-3-phenyl-methylene)-3,4-dihydro-1H-2-oxa-9-thia-fluoren N,N-dimethyl-N-{4-phenyl-spiro[cyclohexane-1,4'-1,4'-dihydro-2'H-3'-oxa-9'-thiafluoren]-4-yl}amine triflate N,N-dimethyl-N-{4-phenyl-spiro[cyclohexane-1,4'-1,4'-dihydro-2'H-3'-oxa-9'-thiafluoren]-4-yl}amine trans-5,6-dihydro-6-hydroxy-2,5,5-trimethyl-7-(2-oxopyrrolidin-1-yl)-5H-thieno<3,2-b>pyran trans-2-bromo-5,6-dihydro-6-hydroxy-5,5-dimethyl-7-(2-oxopyrrolidin-1-yl)-5H-thieno<3,2-b>pyran 5-Cyclohexyl-7-oxo-5-phenyl-7H-thieno[3,2-b]pyran-3-carboxylic acid tert-butyl 2-amino-5,7-dihydro-4H-thieno[2,3-c]pyran-3-carboxylate N-(3-carbamoyl-5,5,7,7-tetramethyl-5,7-dihydro-4H-thieno[2,3-c]pyran-2-yl)-5-methyl-1H-pyrazole-3-carboxamide 5,5-Dimethyl-7-(2-oxo-1-pyrrolidinyl)-5H-thieno[3,2-b]pyran-2-carbonitrile 5,5-Dimethyl-7-(2-oxo-1-pyrrolidinyl)-2-(thiazolin-2-yl)-5-thieno[3,2-b]pyran