돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2244406생성일: 2026년 10월 26일

3-Aminopyridine → 2-Methyl-5-(pyridin-3-ylamino)-thiazole-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/2244406

반응식

참여 물질

역할이름HCID투입량
반응물3-AminopyridineHCID 10009—
반응물Cesium carbonateHCID 10796—
반응물1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
반응물Methyl 5-bromo-2-methyl-1,3-thiazole-4-carboxylateHCID 16427155—
촉매1-Butyl-3-methylimidazolium hexafluorophosphateHCID 2734174—
생성물2-Methyl-5-(pyridin-3-ylamino)-thiazole-4-carboxylic acid methyl esterHCID 6840635994.3%

반응 단계

Dry dioxane (10.00 ml) was degassed by bubbling with argon in an ultrasonic bath, then added to a sealed microwave vial containing a mixture of 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (Xantphos) (0.38 g, 0.66 mmol), palladium dibenzylideneacetone chloroform complex (0.21 g, 0.20 mmol), pyridin-3-ylamine (0.19 g, 2.00 mmol), 5-bromo-2-methyl-thiazole-4-carboxylic acid methyl ester (0.47 g, 2.00 mmol) and cesium carbonate (1.16 g, 6.00 mmol). The mixture was stirred for 10 min, then a few drops of 1-butyl-3-methylimidazolium hexafluorophosphate were added and the vial was irradiated in a microwave oven at 150° C. for 15 min. The volatiles were then removed under vacuum, and the residue was purified by flash chromatography (heptane/ethyl acetate), yielding 2-methyl-5-(pyridin-3-ylamino)-thiazole-4-carboxylic acid methyl ester (0.47 g, 94%), as a yellow solid, MS (ISP): m/e=250.1 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07678815B2
출처 데이터셋uspto-grants-2010_03
ORD IDord-3509a262915e4466867a35269a9d8074
출처 메모uspto-grants-2010_03