phenethyl carbamimidothioate hydrobromide | 6326-49-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: phenethyl carbamimidothioate hydrobromide
• 英文别名: S-phenethyl-isothiourea; hydrobromide；S-Phenaethyl-isothioharnstoff; Hydrobromid；[(2-Phenylethyl)sulfanyl]methanimidamide hydrobromide；2-phenylethyl carbamimidothioate;hydrobromide
• CAS: 6326-49-4
• 化学式: BrH*C₉H₁₂N₂S
• 分子量: 261.186
• InChiKey: MZOXOSCWJWKPGQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.43
• 重原子数：
  13
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  75.2
• 氢给体数：
  3
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  phenethyl carbamimidothioate hydrobromide 在 sodium hydroxide 作用下， 以 乙醇 为溶剂， 反应 2.0h， 生成 2-苯乙硫醇
  参考文献：
  名称：

  Synthesis of N-Glyoxyl Prolyl and Pipecolyl Amides and Thioesters and Evaluation of Their In Vitro and In Vivo Nerve Regenerative Effects

  摘要：

  The recent discovery that small molecule ligands for the peptidyl-prolyl isomerase (PPIase) FKBP12 possess powerful neuroprotective and neuroregenerative properties in vitro and in vivo suggests therapeutic utility for such compounds in neurodegenerative disease. The neurotrophic effects of these compounds are independent of the immunosuppressive pathways by which drugs such as FK506 and rapamycin operate. Previous work by ourselves and other groups exploring the structure-activity relationships (SAR) of small molecules that mimic only the FKBP binding domain portion of FK506 has focused on esters of proline and pipecolic acid. We have explored amide and thioester analogues of these earlier structures and found that they too are extremely potent in promoting recovery of lesioned dopaminergic pathways in a mouse model of Parkinson's disease. Several compounds were shown to be highly effective upon oral administration after lesioning of the dopaminergic pathway, providing further evidence of the potential clinical utility of a variety of structural classes of FKBP12 ligands.

  DOI：

  10.1021/jm010556c
• 作为产物：
  描述：

  乙基溴苯 、 硫脲 以 乙醇 为溶剂， 生成 phenethyl carbamimidothioate hydrobromide
  参考文献：
  名称：

  某些邻苯二酚O-甲基转移酶抑制剂的稳定多底物加合物的合成和评价。

  摘要：

  已经设计了一系列新的甲基化酶抑制剂，其中亲核甲基受体与甲基供体S-腺苷甲硫氨酸的腺苷和/或高半胱氨酸片段连接，形成“多底物加合物”。在当前情况下，已经合成了通过苯乙基硫键连接到5'-硫腺苷或高半胱氨酸的儿茶酚胺类似物，以及相应的甲基ulf盐。这些化合物被检测为儿茶酚O-甲基转移酶的抑制剂，并且腺苷yl盐（4）被发现是该酶的抑制剂。

  DOI：

  10.1021/jm00143a002

文献信息

• Synthesis of difluoromethyl and deuterium-labeled difluoromethyl thioethers from aliphatic electrophiles
  作者：Tianqi Ding、Lvqi Jiang、Wenbin Yi

  DOI：10.1039/c9cc09709k

  日期：——

  described. The transition-metal-free approach, readily available reagents, and mild conditions provide a practical way for the synthesis of difluoromethyl thioethers. By changing the “H” source to the most commonly used “D” sources CD3OD and D2O, this strategy enables efficient synthesis of SCF2D-substituted molecules in good yields with high levels of D incorporation.

  描述了烷基亲电试剂与硫脲和溴代二氟甲基膦酸二乙酯的一锅二氟甲基硫醇化。不含过渡金属的方法，容易获得的试剂和温和的条件为合成二氟甲基硫醚提供了一种实用的方法。通过将“ H”源更改为最常用的“ D”源CD 3 OD和D 2 O，此策略能够以高收率和高D掺入量高效合成SCF 2 D取代分子。
• Design, Synthesis, and Biological Evaluation of Novel, Non-Brain-Penetrant, Hybrid Cannabinoid CB₁R Inverse Agonist/Inducible Nitric Oxide Synthase (iNOS) Inhibitors for the Treatment of Liver Fibrosis
  作者：Malliga R. Iyer、Resat Cinar、Alexis Katz、Michael Gao、Katalin Erdelyi、Tony Jourdan、Nathan J. Coffey、Pal Pacher、George Kunos

  DOI：10.1021/acs.jmedchem.6b01504

  日期：2017.2.9

  We report the design, synthesis, and structure–activity relationships of novel dual-target compounds with antagonist/inverse agonist activity at cannabinoid receptor type 1 (CB1R) and inhibitory effect on inducible nitric oxide synthase (iNOS). A series of 3,4-diarylpyrazolinecarboximidamides were synthesized and evaluated in CB1 receptor (CB1R) binding assays and iNOS activity assays. The novel compounds

  我们报告了新型双靶化合物的设计，合成和结构活性关系，该化合物在1型大麻素受体（CB 1 R）上具有拮抗/反向激动剂活性，并且对诱导型一氧化氮合酶（iNOS）具有抑制作用。合成了一系列3,4-二芳基吡唑啉羧酰亚胺衍生物，并通过CB 1受体（CB 1 R）结合测定和iNOS活性测定进行了评估。被设计为具有有限的脑渗透能力的新型化合物引发了有效的体外CB 1 R拮抗剂活性和iNOS抑制活性。一些关键化合物显示出高的CB 1 R结合亲和力。化合物7在iNOS抑制和CB 1 R拮抗作用介导的纤维化动物模型中，已证实了有效的体内药理活性，例如通过CB 1 Rs拮抗作用介导的食物摄取减少和抗纤维化作用。
• Simple Synthesis of Sulfonyl Chlorides from Thiol Precursors and Derivatives by NaClO2-Mediated Oxidative Chlorosulfonation
  作者：Jiaxi Xu、Zhanhui Yang、Yongpeng Zheng

  DOI：10.1055/s-0033-1339675

  日期：——

  A simple method to synthesize diverse sulfonyl chlorides through NaClO2-mediated oxidative chlorosulfonation of S-alkyl isothiourea salts is presented. The approach features safe operation, environmental friendliness, convenient purification procedures, and delivers high yields of up to 96%. The procedure is also applicable to substrates such as thiols, disulfides, thioacetates, and xanthates. It is

  介绍了一种通过 NaClO2 介导的 S-烷基异硫脲盐氧化氯磺化合成多种磺酰氯的简单方法。该方法操作安全、环境友好、纯化步骤方便，收率高达96%。该程序也适用于底物，如硫醇、二硫化物、硫代乙酸盐和黄原酸盐。它是一种通用且方便的方法，可用于从不同的硫醇前体和衍生物合成各种磺酰氯。
• Synthesis and evaluation of some stable multisubstrate adducts as inhibitors of catechol O-methyltransferase
  作者：Gary L. Anderson、Donald L. Bussolotti、James K. Coward

  DOI：10.1021/jm00143a002

  日期：1981.11

  A new series of methylase inhibitors has been designed in which the nucleophilic methyl acceptor is attached to the adenosine and/or homocysteine fragments of the methyl donor, S-adenosylmethionine, to form a "multisubstrate adduct". In the present case, catecholamine analogues attached through a phenethyl sulfide linkage to 5'-thioadenosine or homocysteine have been synthesized, together with the

  已经设计了一系列新的甲基化酶抑制剂，其中亲核甲基受体与甲基供体S-腺苷甲硫氨酸的腺苷和/或高半胱氨酸片段连接，形成“多底物加合物”。在当前情况下，已经合成了通过苯乙基硫键连接到5'-硫腺苷或高半胱氨酸的儿茶酚胺类似物，以及相应的甲基ulf盐。这些化合物被检测为儿茶酚O-甲基转移酶的抑制剂，并且腺苷yl盐（4）被发现是该酶的抑制剂。
• Convenient and Environment-Friendly Synthesis of Sulfonyl Chlorides from S-Alkylisothiourea Salts via N-Chlorosuccinimide Chlorosulfonation
  作者：Jiaxi Xu、Zhanhui Yang

  DOI：10.1055/s-0033-1338743

  日期：——

  the byproduct succinimide from ‘waste water’ can be conveniently converted into the starting reagent N-chlorosuccinimide with sodium hypochlorite (bleach) to make the method sustainable. A convenient, practical, and environmentally friendly method for the synthesis of sulfonyl chlorides has been developed. Structurally diverse sulfonyl chlorides were synthesized in moderate to excellent yields from

  摘要 已经开发了一种方便，实用和环境友好的合成磺酰氯的方法。由S-烷基异硫脲盐以中等至优异的产率合成结构多样的磺酰氯，其可以容易地由易于获得的烷基卤化物或甲磺酸酯和廉价的硫脲通过N-氯代琥珀酰亚胺氯磺化制备。在大规模合成中，可以将来自“废水”的副产物琥珀酰亚胺与次氯酸钠（漂白剂）方便地转化为起始试剂N-氯琥珀酰亚胺，以使该方法具有可持续性。 已经开发了一种方便，实用和环境友好的合成磺酰氯的方法。由S-烷基异硫脲盐以中等至优异的产率合成结构多样的磺酰氯，其可以容易地由易于获得的烷基卤化物或甲磺酸酯和廉价的硫脲通过N-氯代琥珀酰亚胺氯磺化制备。在大规模合成中，可以将来自“废水”的副产物琥珀酰亚胺与次氯酸钠（漂白剂）方便地转化为起始试剂N-氯琥珀酰亚胺，以使该方法具有可持续性。