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(Z)-2-[(methylsulfonyl)methylidene]pyrrolidino[2,1-c]thiazolidine | 1190227-99-6

中文名称
——
中文别名
——
英文名称
(Z)-2-[(methylsulfonyl)methylidene]pyrrolidino[2,1-c]thiazolidine
英文别名
(3Z,7aS)-3-(methylsulfonylmethylidene)-5,6,7,7a-tetrahydro-1H-pyrrolo[1,2-c][1,3]thiazole
(Z)-2-[(methylsulfonyl)methylidene]pyrrolidino[2,1-c]thiazolidine化学式
CAS
1190227-99-6
化学式
C8H13NO2S2
mdl
——
分子量
219.329
InChiKey
RMBIDLBFMFJPTA-VQKCLUMFSA-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

物化性质

  • 沸点:
    407.5±44.0 °C(Predicted)
  • 密度:
    1.38±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    71.1
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    (Z)-2-[(methylsulfonyl)methylidene]pyrrolidino[2,1-c]thiazolidine盐酸 作用下, 以 为溶剂, 反应 15.0h, 生成 甲磺酰乙酸 、 (S)-prolinethiol hydrochloride
    参考文献:
    名称:
    通过噻唑啉盐多功能合成仲 2-氨基硫醇和/或其二硫化物
    摘要:
    通过使用二硫代乙酸甲酯作为硫源,已将市售的 β-氨基醇转化为各种仲 β-氨基硫醇和/或其二硫化物。该转化涉及作为通用关键中间体的噻唑啉盐,它可以通过改变杂环和 N-烷基化剂上的取代基轻松调节产品结构。 (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany , 2009)
    DOI:
    10.1002/ejoc.200900514
  • 作为产物:
    描述:
    (S)-thioacetylprolinol 、 甲基磺酰氯三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 0.5h, 以57%的产率得到(Z)-2-[(methylsulfonyl)methylidene]pyrrolidino[2,1-c]thiazolidine
    参考文献:
    名称:
    通过噻唑啉盐多功能合成仲 2-氨基硫醇和/或其二硫化物
    摘要:
    通过使用二硫代乙酸甲酯作为硫源,已将市售的 β-氨基醇转化为各种仲 β-氨基硫醇和/或其二硫化物。该转化涉及作为通用关键中间体的噻唑啉盐,它可以通过改变杂环和 N-烷基化剂上的取代基轻松调节产品结构。 (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany , 2009)
    DOI:
    10.1002/ejoc.200900514
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文献信息

  • Versatile Synthesis of Secondary 2-Amino Thiols and/or Their Disulfides via Thiazolinium Salts
    作者:Guillaume Mercey、Jean-François Lohier、Annie-Claude Gaumont、Jocelyne Levillain、Mihaela Gulea
    DOI:10.1002/ejoc.200900514
    日期:2009.9
    Commercially available β-amino alcohols have been transformed into various secondary β-amino thiols and/or their disulfides by using methyl dithioacetate as a source of sulfur. The transformation involves a thiazolinium salt as a versatile key intermediate, which enables easy modulation of the product structure by varying the substituents on the heterocycle and the N-alkylating agent.(© Wiley-VCH Verlag
    通过使用二硫代乙酸甲酯作为硫源,已将市售的 β-氨基醇转化为各种仲 β-氨基硫醇和/或其二硫化物。该转化涉及作为通用关键中间体的噻唑啉盐,它可以通过改变杂环和 N-烷基化剂上的取代基轻松调节产品结构。 (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany , 2009)
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同类化合物

4H-吡咯并[2.3-d][1,3]噻唑-5-羧酸乙酯 4H-吡咯并[2,3-d]噻唑-5-羧酸 4H-吡咯并[2,3-d]噻唑 (7aS)-1-(1-cyanoethenyl)tetrahydro-1H,3H-pyrrolo[1,2-c]thiazole-3-thione 4-methyl-4,6-dihydro-5H-thiazolo[5‘,4‘:4,5]pyrrolo[2,3-d]pyridazin-5-one 3-((2,4-dimethyl-5-oxo-4H-thiazolo[5’,4’:4,5]pyrrolo[2,3-d]pyridazin-6(5H)-yl)methyl)benzonitrile 7-propyl-7H-3,4-dithia-1,6,7-triazacyclopenta[a]pentalene 7-propyl-2,5-bis(trimethylstannyl)-7H-3,4-dithia-1,6,7-triazacyclopenta[a]pentalene 4-methyl-4H-pyrrolo[2,3-d]thiazole-5-carboxylic acid 3-morpholino-4-(2,4,5-trimethyl-4H-pyrrolo[3,2-d][1,3]thiazol-6-yl)cyclobut-3-ene-1,2-dione (S)-3-thia-1-azabicyclo[3.3.0]octan-2-one 3,3-dioxide methyl 4H-pyrrolo[2,3-d]thiazole-5-carboxylate (4H-pyrrolo[2,3-d]thiazol-5-yl)methanol 5-methyl-4H-pyrrolo[2,3-d]thiazole tert-butyl 2-amino-4H-pyrrolo[3,2-d]thiazole-4-carboxylate 2-ethoxycarbonylamino-4-methyl-4H-pyrrolo[3,2-d]thiazole-5-carboxylic acid methyl ester (4-methyl-6-nitro-4H-pyrrolo[2,3-d]thiazol-2-yl)-carbamic acid ethyl ester 2-ethoxycarbonylamino-4-methyl-4H-pyrrolo[3,2-d]thiazole-5-carboxylic acid ethyl ester (5-bromo-4-methyl-6-nitro-4H-pyrrolo[3,2-d]thiazol-2-yl)-carbamic acid ethyl ester 2-Ethoxycarbonylamino-4-methylpyrrolo<3,2-d>thiazol (Z)-2-[(methylsulfonyl)methylidene]pyrrolidino[2,1-c]thiazolidine (5-bromo-4-methyl-6-nitro-4H-pyrrolo[2,3-d]thiazol-2-yl)-carbamic acid ethyl ester ethyl 2-methyl-4H-pyrrolo[3,2-d]thiazole-5-carboxylate ethyl 5-methyl-5H-pyrrolo[3,4-d]thiazolo-2-carboxylate 2-phenyl-4H-pyrrolo[3,2-d]thiazole-5-carboxylic acid ethyl ester 5-benzyl-4H-pyrrolo[2,3-d]thiazole 4-(4H-pyrrolo[2,3-d]thiazol-5-yl)pyridin-2-ylamine ethyl 4H-pyrrolo[3,2-d]thiazole-5-carboxylate 2,6-dibromo-4-(2-octyldodecyl)-4H-pyrrolo[3,2-d:4,5-d]bisthiazole tetrahydro-pyrrolo[1,2-c]thiazole-3-thione (-)-(1R,7aS)-1-methyltetrahydropyrrolo[1,2-c]thiazol-3(1H)-thione (-)-(1S,7aS)-1-methyltetrahydropyrrolo[1,2-c]thiazol-3(1H)-thione methyl (2R,6R,7R,8S,11R)-5-oxo-11-phenyl-10-thia-1-azatricyclo[6.3.0.02,6]undecane-7-carboxylate (2R,6R,7R,8S,11R)-11-phenyl-7-[(E)-2-phenylethenyl]-10-thia-1-azatricyclo[6.3.0.02,6]undecan-5-one N-[[4-(propan-2-ylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide N-[[4-(pyridin-2-ylmethylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide N-[[4-(morpholine-4-carbonyl)cyclohexyl]methyl]-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide N-[[4-(thiophen-2-ylmethylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxamide N-[[4-(pyridin-2-ylmethylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide N-[[4-(morpholine-4-carbonyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide N-[[4-(cyclopropylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide N-[[4-(furan-2-ylmethylcarbamoyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide N-[[4-(pyrrolidine-1-carbonyl)cyclohexyl]methyl]-4H-pyrrolo[2,3-d][1,3]thiazole-5-carboxamide (1S,2S,7S,8R)-10-[2-[[3-chloro-5-(trifluoromethyl)pyridin-2-yl]amino]ethyl]-7-[(E)-2-phenylethenyl]-4-thia-6,10-diazatricyclo[6.3.0.02,6]undecane-9,11-dione (1S,2S,7R,8R)-10-[2-[[3-chloro-5-(trifluoromethyl)pyridin-2-yl]amino]ethyl]-7-[(E)-2-phenylethenyl]-4-thia-6,10-diazatricyclo[6.3.0.02,6]undecane-9,11-dione 4-[(3,4-Dichlorophenyl)methyl]pyrrolo[2,3-d][1,3]thiazole-5-carboxylic acid 2-(4H-pyrrolo[2,3-d][1,3]thiazol-5-yl)acetic acid Methyl 4-(3,4-dichlorobenzyl)-2-methyl-4 H-pyrrolo[3,2-d ][1,3]thiazole-5-carboxylate Ethyl 4-[(3,4-dichlorophenyl)methyl]pyrrolo[2,3-d][1,3]thiazole-5-carboxylate methyl 4-(3,4-dichlorobenzyl)-4H-pyrrolo[3,2-d][1,3]thiazole-5-carboxylate