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6-(benzyloxycarbonyl)amino-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-7H-pyrano<2,3-d>pyrimidin-7-one | 223718-61-4

中文名称
——
中文别名
——
英文名称
6-(benzyloxycarbonyl)amino-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-7H-pyrano<2,3-d>pyrimidin-7-one
英文别名
benzyl N-(1,3-dimethyl-2,4,7-trioxopyrano[2,3-d]pyrimidin-6-yl)carbamate
6-(benzyloxycarbonyl)amino-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-7H-pyrano<2,3-d>pyrimidin-7-one化学式
CAS
223718-61-4
化学式
C17H15N3O6
mdl
——
分子量
357.323
InChiKey
JPADPASTRGXMMK-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):
    0.9
  • 重原子数:
    26
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    105
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    6-(benzyloxycarbonyl)amino-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-7H-pyrano<2,3-d>pyrimidin-7-one 在 palladium on activated charcoal 环己烯 作用下, 以 乙醇 为溶剂, 反应 0.33h, 以94%的产率得到6-amino-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-7H-pyrano<2,3-d>pyrimidin-7-one
    参考文献:
    名称:
    2-(苄氧基羰基)氨基-3-二甲基氨基丙烯酸甲酯的合成。三取代吡咯,3-氨基-2 H-吡喃-2-酮,稠合的2 H-吡喃-2-酮和4 H-吡啶-4-酮的合成
    摘要:
    由N-(苄氧基羰基)甘氨酸甲酯(1)和叔丁氧基双(二甲基氨基)甲烷制得2-(苄氧基羰基)亚氨基-3-二甲基氨基丙酸甲酯(2),并用作制备取代的3-(苄氧基羰基)的试剂。氨基-4- ħ喹嗪-4-酮5和6,-2 ħ吡喃-2-酮17-19,-2 ħ -1-苯并吡喃-2-酮28-31,和-naphthopyrans 32-35, - 2 H-吡喃并[3,2 - c ]吡啶-2,5-二酮46,-吡喃并- [4,3 - b ]吡喃-2,5-二酮47,-pyrano [3,2 - c ]苯并吡喃-2,5-二酮48,-pyrano [2,3 - c ] pyrazol -6-ones 49和50,-pyrano [2,3 - d ] pyrirnidin-7 -酮51层52的衍生物。在2与1,3-二酮的反应中,形成了三取代的吡咯14-16。选择性除去苄氧羰基的由猫alytic转移氢化用Pd / C在环己烯
    DOI:
    10.1002/jhet.5570360135
  • 作为产物:
    参考文献:
    名称:
    2-(苄氧基羰基)氨基-3-二甲基氨基丙烯酸甲酯的合成。三取代吡咯,3-氨基-2 H-吡喃-2-酮,稠合的2 H-吡喃-2-酮和4 H-吡啶-4-酮的合成
    摘要:
    由N-(苄氧基羰基)甘氨酸甲酯(1)和叔丁氧基双(二甲基氨基)甲烷制得2-(苄氧基羰基)亚氨基-3-二甲基氨基丙酸甲酯(2),并用作制备取代的3-(苄氧基羰基)的试剂。氨基-4- ħ喹嗪-4-酮5和6,-2 ħ吡喃-2-酮17-19,-2 ħ -1-苯并吡喃-2-酮28-31,和-naphthopyrans 32-35, - 2 H-吡喃并[3,2 - c ]吡啶-2,5-二酮46,-吡喃并- [4,3 - b ]吡喃-2,5-二酮47,-pyrano [3,2 - c ]苯并吡喃-2,5-二酮48,-pyrano [2,3 - c ] pyrazol -6-ones 49和50,-pyrano [2,3 - d ] pyrirnidin-7 -酮51层52的衍生物。在2与1,3-二酮的反应中,形成了三取代的吡咯14-16。选择性除去苄氧羰基的由猫alytic转移氢化用Pd / C在环己烯
    DOI:
    10.1002/jhet.5570360135
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文献信息

  • The synthesis of methyl 2-(benzyloxycarbonyl)amino-3-dimethylaminopropenoate. The synthesis of trisubstituted pyrroles, 3-amino-2<i>H</i>-pyran-2-ones, fused 2<i>H</i>-pyran-2-ones and 4<i>H</i>-pyridin-4-ones
    作者:Renata Toplak、Jurij Svete、Branko Stanovnik、Simona GoliČ Grdadolnik
    DOI:10.1002/jhet.5570360135
    日期:1999.1
    Methyl 2-(benzyloxycarbonyl)aimno-3-dimemylaminopropenoate (2) was prepared from methyl N-(benzyloxycarbonyl)glycinate (1) and t-butoxybis(dimethylamino)methane, and used as a reagent for preparation of substituted 3-(benzyloxycarbonyl)amino-4H-quinolizin-4-ones 5 and 6, −2H-pyran-2-ones 17–19, −2H-1-benzopyran-2-ones 28–31, and -naphthopyrans 32–35, −2H-pyrano[3,2-c]pyridine-2,5-dione 46, -pyrano-[4
    由N-(苄氧基羰基)甘氨酸甲酯(1)和叔丁氧基双(二甲基氨基)甲烷制得2-(苄氧基羰基)亚氨基-3-二甲基氨基丙酸甲酯(2),并用作制备取代的3-(苄氧基羰基)的试剂。氨基-4- ħ喹嗪-4-酮5和6,-2 ħ吡喃-2-酮17-19,-2 ħ -1-苯并吡喃-2-酮28-31,和-naphthopyrans 32-35, - 2 H-吡喃并[3,2 - c ]吡啶-2,5-二酮46,-吡喃并- [4,3 - b ]吡喃-2,5-二酮47,-pyrano [3,2 - c ]苯并吡喃-2,5-二酮48,-pyrano [2,3 - c ] pyrazol -6-ones 49和50,-pyrano [2,3 - d ] pyrirnidin-7 -酮51层52的衍生物。在2与1,3-二酮的反应中,形成了三取代的吡咯14-16。选择性除去苄氧羰基的由猫alytic转移氢化用Pd / C在环己烯
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乙基7'-氨基-6-氟-2,2',4'-三羰基-1,1',2,2',3',4'-六氢螺[吲哚-3,5'-吡喃并[2,3-d]嘧啶]-6'-羧酸酯 7H-吡喃并[2,3-d]嘧啶-7-酮 7H-吡喃并[2,3-d]嘧啶 7,8-二氢-5H-吡喃并[4,3-D]嘧啶-2-胺 5H-吡喃并[4,3-d]嘧啶 5H-吡喃并[2,3-d]嘧啶 2H-吡喃并[2,3-d]嘧啶-6-甲腈,7-氨基-1,3,4,5-四氢-5-(4-甲氧苯基)-2,4-二羰基- 2,4-二氯-7,8-二氢-5H-吡喃[4,3-d]嘧啶 1H-吡喃并[3,4-d]嘧啶 1H-吡喃并[3,2-d]嘧啶 4-(4-methoxyaniline)-5-(phenyl)-8,9-dihydro-5H-chromeno[2,3-d]pyrimidin-6(7H)-one 4-cyclohexyl-2-phenyl-7,8-dihydro-6H-pyranol[3,2-d]pyrimidine 1,3-Bis(p-tolyl)-5-(2'-hydroxyphenyl)-7-methyl-4-oxo-1,2,3,4-tetrahydro-2-thioxo-5H-pyrano<2,3-d>pyrimidine 7,8-dihydro-3H-pyrano[4,3-d]pyrimidin-4(5H)-one 7-amino-2,3,4,5-tetrahydro-5-(3-hydroxyphenyl)-1,3-dimethyl-2,4-dioxo-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile 3-benzyl-6,6,9-trimethyl-6a,7,8,9,10,10a-hexahydro-6H-isochromeno[3,4-d]pyrimidin-1-ol 7'-amino-1-ethyl-2,4'-dioxo-2'-thioxo-1',2',3',4'-tetrahydrospiro[indoline-3,5'-pyrano[2,3-d] pyrimidine]-6'-carbonitrile 7'-amino-2,4'-dioxo-2'-thioxo-1',2',3',4'-tetrahydro-2H-spiro[acenaphthylene-1,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile (3-(((2-(4-(but-2-ynamido)-2-methyl-1H-indol-1-yl)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-yl)amino)methyl)phenyl)boronic acid 7-amino-5-(2,3-dimethoxyphenyl)-1,3-dimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile 7'-amino-5-chloro-1',3'-dimethyl-2,2',4'-trioxo-1',2',3',4'-tetrahydrospiro[indoline-3,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile 7-amino-5-(4-bromophenyl)-1,3-dimethyl-2,4-dioxo-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carbonitrile 7-amino-5-(4-methoxyphenyl)-1,3-dimethyl-2,4-dioxo-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]-pyrimidine-6-carbonitrile 7,8-dihydro-5H-pyrano[4,3-d]pyrimidine ethyl 2,8-dimethyl-10-phenyl-10H-pyrano[3,2-e][1,2,4]triazolo[1,5-c] pyrimidine-9-carboxylate ethyl 10-(4-methoxyphenyl)-2,8-dimethyl-10H-pyrano[3,2-e][1,2,4]triazolo[1,5-c] pyrimidine-9-carboxylate ethyl 3-{[3-(4-methoxyphenyl)isoxazol-5-yl]methyl}-2,7-dimethyl-4-oxo-5-(p-tolyl)-3,5-dihydro-4H-pyrano[2,3-d]pyrimidine-6-carboxylate 2-thioxo-2,3,7,8-tetrahydro-1H-pyrano[4.3-d]pyrimidin-4(5H)-one 7-amino-2,4-dioxo-5-(m-tolyl)-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carbonitrile Ethyl 7-amino-5-(4-hydroxyphenyl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carboxylate 7-amino-5-(3-chlorophenyl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile 7-amino-5-(2,4-di-chlorophenyl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile 7-amino-5-(4-(dimethylamino)phenyl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile Ethyl 7-amino-5-(3,4-dimethoxyphenyl)-2,4-dioxo-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carboxylate 7-amino-5-(3,4-dimethoxyphenyl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carbonitrile ethyl-7-amino-5-(3-nitrphenyl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d]pyrimidine-6-carboxylate Ethyl 7-amino-5-(4-nitrophenyl)-2,4-dioxo-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carboxylate Ethyl 7-amino-5-(4-methylphenyl)-2,4-dioxo-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carboxylate 7'-amino-5-chloro-2,2',4'-trioxo-1',2',3',4'-tetrahydrospiro[indoline-3,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile 4-tert-butyl-2-phenyl-7,8-dihydro-6H-pyranol[3,2-d]pyrimidine 6-benzamido-2,3-dihydro-5-methyl-1,3-di(p-chlorophenyl)-2-thioxo-4H-pyrano[2,3-d]pyrimidine-4,7(1H)-dione 6-benzamido-2,3-dihydro-5-methyl-1,3-diphenyl-2-thioxo-4H-pyrano[2,3-d]pyrimidine-4,7(1H)-dione 4-phenylhexahydro-1H-pyrano[2,3-d]pyrimidin-2(8aH)-one 4-(4-methoxyphenyl)hexahydro-1H-pyrano[2,3-d]pyrimidin-2(8aH)-one 7-amino-1,3-dimethyl-2,4-dioxo-5-phenyl-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carbonitrile 7'‑amino‑2,4′‑dioxo‑2′‑thioxo‑1′,2′,3′,4′‑tetrahydrospiro[indoline‑3,5'‑pyrano[2,3‑d]pyrimidine]‑6'‑carbonitrile 7-Amino-5-(1H-indol-3-yl)-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrano[2,3-d] pyrimidine-6-carbonitrile methyl 2-amino-5,7-dioxospiro[1'-methyl-3'H-indol-3',4-4H-5,6,7,8-tetrahydropyrano[2,3-d]pyramidine]-1'H-2'-one-3-carboxylate 7-benzyl-7-methyl-4-phenyl-3,4,7,8-tetrahydro-1H-pyrano[4,3-d]pyrimidine-2,5-dione 7,7-dimethyl-4-phenyl-2-thioxo-1,2,3,4,7,8-hexahydro-pyrano[4,3-d]pyrimidin-5-one