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HRID 928738생성일: 2026년 10월 27일

5-Bromo-1-methyl-1H-imidazole → (1-Methyl-1H-imidazol-5-yl)(thiazol-5-yl)methanone

https://huagongshe.com/reaction/928738

반응식

참여 물질

역할이름HCID투입량
반응물5-Bromo-1-methyl-1H-imidazoleHCID 1515258—
반응물N-Methoxy-N-methyl-1,3-thiazole-5-carboxamideHCID 25307138—
반응물HCID 178418443HCID 178418443—
용매DichloromethaneHCID 6344—
생성물(1-Methyl-1H-imidazol-5-yl)(thiazol-5-yl)methanoneHCID 86715592—

반응 단계

To a solution of 5-bromo-1-methyl-1H-imidazole (1.14 g, 7.11 mmol) in DCM was added ethyl magnesium bromide (2.34 mL, 7.11 mmol; 3.0 M in diethyl ether) dropwise over a 10 minute period. The resulting pale yellow solution was stirred at room temperature for 15 minutes, cooled in an ice bath to 0° C. and N-methoxy-N-methylthiazole-5-carboxamide (1.02 g, 5.92 mmol, Intermediate 11: step a) dissolved in DCM (3 mL) was added dropwise. The cold bath was removed and the reaction mixture stirred at room temperature for 48 hours. To the resulting yellow suspension was added water followed by 6 M aqueous HCl to a neutral pH (pH=6-7). The aqueous mixture was extracted with DCM, dried over Na2SO4, filtered and concentrated. Et2O was added and the mixture sonicated. The precipitate was collected by filtration and dried to provide the title compound as a tan solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09290476B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-605fe22491404975a4da403d95aa5b3f
출처 메모uspto-grants-2016_03