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【结 构 式】

【分子编号】53535

【品名】N-[(Z)-{[2-oxo-2-(3-pyridinyl)ethyl]sulfanyl}(propylamino)methylidene]guanidine

【CA登记号】n/a

【 分 子 式 】C12H17N5OS

【 分 子 量 】279.36608

【元素组成】C 51.59% H 6.13% N 25.07% O 5.73% S 11.48%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(III)

The reaction of N1-amidino-N3-propylthiourea (I) with 2-bromo-1-(3-pyridyl)ethanone (II) in ethanol/acetone gives the N1-amidino-S-[2-oxo-2-(3-pyridyl)ethyl]-N3-propylisothiourea (III), which without isolation is cyclized to the target aminothiazole by means of TEA.

1 Sorensen, A.R.; Engelhardt, S.; Kurtzhals, P.; Urso, B.; Bowler, A.N.; 2,4-Diaminothiazoles: A novel class of glycogen synthase kinase-3 (GSK-3) inhibitors. 11th RSC-SCI Med Chem Symp (Sept 9 2001, Cambridge) 2001, Abst P20.
2 Olesen, P.H.; Kurtzhals, P.; Bowler, A.N.; Soerensen, A.R.; Worsaae, H.; Hansen, B.F. (Novo Nordisk A/S); 2,4-Diaminothiazole derivs.. WO 0156567 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 53534 1-Amidino-3-propyl-2-thiourea n/a C5H12N4S 详情 详情
(II) 53058 (2-benzyl-4,8,8-trimethyl-6,10-dioxa-2-azaspiro[4.5]dec-4-yl)methyl azide; 4-(azidomethyl)-2-benzyl-4,8,8-trimethyl-6,10-dioxa-2-azaspiro[4.5]decane n/a C18H26N4O2 详情 详情
(III) 53535 N-[(Z)-{[2-oxo-2-(3-pyridinyl)ethyl]sulfanyl}(propylamino)methylidene]guanidine n/a C12H17N5OS 详情 详情
Extended Information