Identification | Back Directory | [Name]
Ethyl 2-(4-(tert-butoxycarbonyl)piperazin-1-yl)thiazole-4-carboxylate | [CAS]
867065-53-0 | [Synonyms]
Ethyl 2-(4-Boc-1-piperazinyl)thiazole-4-carboxylate Ethyl 2-(4-(tert-butoxycarbonyl)piperazin-1-yl)thiazole-4-carboxylate tert-butyl 4-(4-(ethoxycarbonyl)thiazol-2-yl)piperazine-1-carboxylate 4-(4-Ethoxycarbonylthiazol-2-yl)piperazine-1-carboxylic acid tert-butyl ester ethyl 2-[4-[(2-methylpropan-2-yl)oxycarbonyl]piperazin-1-yl]-1,3-thiazole-4-carboxylate 1-Piperazinecarboxylic acid, 4-[4-(ethoxycarbonyl)-2-thiazolyl]-, 1,1-dimethylethyl ester | [Molecular Formula]
C15H23N3O4S | [MDL Number]
MFCD08445626 | [MOL File]
867065-53-0.mol | [Molecular Weight]
341.43 |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of ethyl 2-(4-(tert-butoxycarbonyl)piperazin-1-yl)thiazole-4-carboxylate from ethyl 2-bromothiazole-4-carboxylate and N-BOC-piperazine: ethyl N-BOC-piperazine (1.8 g, 10 mmol), ethyl 2-bromothiazole-4-carboxylate (2.36 g, 10 mmol) and N,N-diisopropylethylamine (DIPEA. 2.02 g, 20 mmol) were dissolved in 1,4-dioxane (15 mL). The reaction mixture was stirred at 100°C overnight. Upon completion of the reaction, it was extracted with ethyl acetate (EA) and the organic phase was washed with saturated saline. Purification by fast column chromatography (eluent: petroleum ether/ethyl acetate = 5:1 to 3:1) afforded a yellow solid product (3.0 g, 88% yield). | [References]
[1] Patent: US2018/141923, 2018, A1. Location in patent: Paragraph 0599; 0600; 0601 [2] Patent: WO2008/83238, 2008, A2. Location in patent: Page/Page column 112 [3] Patent: WO2018/26890, 2018, A1. Location in patent: Paragraph 0479; 0480 |
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