5-羟基-1,3-苯并氧硫杂环戊烷-2-酮 | 7735-56-0

• 物质功能分类: 化学试剂 - 有机试剂 - 硫醇/硫酚
• 分子结构分类: 有机化合物 - 苯类化合物 - 酚类
• 中文名称: 5-羟基-1,3-苯并氧硫杂环戊烷-2-酮
• 中文别名: HBT_西亚试剂；5-羟基-1,3-苯并噁硫醇-2-酮
• 英文名称: 5-hydroxy-1,3-benzoxathiol-2-one
• 英文别名: 5-hydroxybenzo[d][1,3]oxathiol-2-one；5-Hydroxy-1,3-benzoxathiol-2-on
• CAS: 7735-56-0
• 化学式: C₇H₄O₃S
• mdl: MFCD00460208
• 分子量: 168.173
• InChiKey: HDSYJLOFQVPBJM-UHFFFAOYSA-N

物化性质

• 熔点：
  173-175 °C
• 沸点：
  375.4±44.0 °C(Predicted)
• 密度：
  1.617±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  11
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  71.8
• 氢给体数：
  1
• 氢受体数：
  4

安全信息

• 危险等级：
  IRRITANT
• 海关编码：
  2930909090

反应信息

• 作为反应物：
  描述：

  5-羟基-1,3-苯并氧硫杂环戊烷-2-酮 在 一水合肼 作用下， 以 乙醇 为溶剂， 生成 hydrazinecarbothioic acid S-(2,5-dihydroxy-phenyl) ester
  参考文献：
  名称：

  Matveev,L.G. et al., Journal of general chemistry of the USSR, 1975, vol. 45, p. 657 - 660

  摘要：

  DOI：
• 作为产物：
  描述：

  hydrazinecarbothioic acid S-(2,5-dihydroxy-phenyl) ester 生成 5-羟基-1,3-苯并氧硫杂环戊烷-2-酮
  参考文献：
  名称：

  MATVEEV L. G.; PITINA M. R.; SHVETSOV-SHILOVSKIJ N. I.; KULIKOV N. S., VNII XIM. SREDSTV ZASHCHITY PACT. M., 1975, 20 S., BIBLIOGR. 6 NAZV. (RUK+

  摘要：

  DOI：

文献信息

• [EN] NOVEL PIPERAZINYL-PYRAZINONE DERIVATIVES FOR THE TREATMENT OF 5-HT2A RECEPTOR-RELATED DISORDERS<br/>[FR] NOUVEAUX DERIVES DE PIPERAZINYL-PYRAZINONE POUR LE TRAITEMENT DES TROUBLES LIES AU RECEPTEUR 5-HT2A
  申请人：BIOVITRUM AB

  公开号：WO2004009586A1

  公开（公告）日：2004-01-29

  Compounds of the general formula (I): (I)wherein m, n, R1, R2, R3 and R4 are as described in the specification. Further included are pharmaceutical compositions comprising the compounds, processes for their preparation, as well as the use of the compounds for the preparation of a medicament for the treatment of 5-HT2A receptor-related disorders or medical conditions.

  通式（I）的化合物：（I）其中m、n、R1、R2、R3和R4如规范中所述。还包括包含这些化合物的药物组合物，它们的制备方法，以及利用这些化合物制备用于治疗5-HT2A受体相关疾病或医疗状况的药物的用途。
• [EN] COMPOUNDS CONTAINING POLYSUBSTITUTED BENZO[D][1,3]OXATHIOLE, BENZO[D][1,3]OXATHIOLE 3-OXIDE OR BENZO[D][1,3]OXATHIOLE 3,3-DIOXIDE AND METHODS/USES THEREOF AS AGONISTS OF G PROTEIN-COUPLED RECEPTOR 119<br/>[FR] COMPOSÉS CONTENANT DU BENZO[D][1,3]OXATHIOLE, BENZO[D][1,3]OXATHIOLE 3-OXYDE OU DU BENZO[D][1,3]OXATHIOLE 3,3-DIOXYDE POLYSUBSTITUÉ, ET LEURS PROCÉDÉS/UTILISATIONS EN TANT QU'AGONISTES DU RÉCEPTEUR 119 COUPLÉ À LA PROTÉINE G
  申请人：PRAMANA PHARMACEUTICALS INC

  公开号：WO2019104418A1

  公开（公告）日：2019-06-06

  There are provided compounds having formula (I), in which: X1 and X2 are selected from certain combinations of O, S, SO and SO2; X3 is selected from CH, CF and N; X4 is selected from CH and N; X6, X6' and X6'' are selected from H, halogen, and certain alkyl, haloalkyl, alkoxy, hydroxyalkyl, and amide groups; X7 and X7' are selected from H, halogen, and certain alkyl, haloalkyl, alkoxy, hydroxyalkyl, aminoalkyl and amide groups, or both X7 and X7' together form a cycloalkyl or heterocycle; and A is selected from certain optionally substituted, alkoxy, piperazinyl and pyrrolidinyl groups. Also provided are compositions comprising these compounds, as well as uses/methods related thereto, including treatment of diseases and conditions associated with GPR119 dysregulation, Type 2 diabetes mellitus, and related metabolic disorders. (I)

  提供具有化学式（I）的化合物，其中：X1和X2从O、S、SO和SO2的某些组合中选择；X3从CH、CF和N中选择；X4从CH和N中选择；X6、X6'和X6''从H、卤素以及某些烷基、卤代烷基、烷氧基、羟基烷基和酰胺基中选择；X7和X7'从H、卤素以及某些烷基、卤代烷基、烷氧基、羟基烷基、氨基烷基和酰胺基中选择，或者X7和X7'一起形成环烷基或杂环；A从某些可选择取代的烷氧基、哌嗪基和吡咯烷基中选择。还提供包含这些化合物的组合物，以及与之相关的用途/方法，包括治疗与GPR119失调、2型糖尿病以及相关代谢紊乱相关的疾病和症状。
• 벤조[d][1,3]옥사티올, 벤조[d][1,3]옥사티올 3-옥사이드 또는 벤조[d][1,3]옥사티올 3,3-디옥사이드를 함유하는 화합물 및 Ｇ 단백질 커플링된 수용체 119의 작용제로서 이의 방법/용도
  申请人：PRAMANA PHARMACEUTICALS INC. 프라마나 파마슈티컬스 인크.(520180806346)

  公开号：KR20190015535A

  公开（公告）日：2019-02-13

  본 발명에서는 벤조[d][1,3]옥사티올, 벤조[d][1,3]옥사티올 3-옥사이드, 및 벤조[d][1,3]옥사티올 3,3-디옥사이드를 함유하는 화합물 뿐만 아니라 GPR119 이상조절과 관련된 질환 및 병태, 2형 진성 당뇨병, 및 관련된 대사 장애의 치료를 포함하는 상기 화합물에 관한 관련된 용도/방법이 제공된다.

  本发明提供了一种含有苯并[d][1,3]噻二唑、苯并[d][1,3]噻二唑-3-氧化物和苯并[d][1,3]噻二唑-3,3-二氧化物的化合物，以及与GPR119调节和相关的疾病和病理、2型糖尿病以及相关代谢紊乱的治疗有关的该化合物的相关用途/方法。
• Estrogen receptor modulators
  申请人：——

  公开号：US20030225132A1

  公开（公告）日：2003-12-04

  The present invention relates to compounds and derivatives thereof, their synthesis, and their use as estrogen receptor modulators. The compounds of the instant invention are ligands for estrogen receptors and as such may be useful for treatment or prevention of a variety of conditions related to estrogen functioning including: bone loss, bone fractures, osteoporosis, cartilage degeneration, endometriosis, uterine fibroid disease, hot flashes, increased levels of LDL cholesterol, cardiovascular disease, impairment of cognitive functioning, cerebral degenerative disorders, restenosis, gynecomastia, vascular smooth muscle cell proliferation, obesity, incontinence, and cancer, in particular of the breast, uterus and prostate.

  本发明涉及化合物及其衍生物，它们的合成以及它们作为雌激素受体调节剂的用途。本发明的化合物是雌激素受体的配体，因此可能对治疗或预防与雌激素功能相关的多种疾病条件有用，包括：骨质疏松、骨折、骨质疏松症、软骨退化、子宫内膜异位症、子宫肌瘤病、潮热、低密度脂蛋白胆固醇水平升高、心血管疾病、认知功能障碍、脑退行性疾病、再狭窄、男性乳房增大、血管平滑肌细胞增殖、肥胖、尿失禁和癌症，尤其是乳腺、子宫和前列腺癌。
• 5-Substituted-benzoxathiol-2-ones
  申请人：The Dow Chemical Company

  公开号：US04349685A1

  公开（公告）日：1982-09-14

  Novel, biologically active, 5-substituted-1,3-benzoxathiol-2-ones are prepared by the reaction of 5-hydroxy-1,3-benzoxathiol-2-one with a substituted isocyanate in the presence of an activating agent and an appropriate organic solvent. The novel compounds are suitable for use as fungicides and as the active constituents in fungicidal compositions.

  通过在适当的有机溶剂存在下，将5-羟基-1,3-苯并噻吩-2-酮与取代异氰酸酯反应制备出一种新型的具有生物活性的5-取代-1,3-苯并噻吩-2-酮。这些新型化合物适用于用作杀真菌剂以及真菌杀菌剂组合物中的活性成分。

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