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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1685292생성일: 2026년 10월 26일

Water → N-(6-chloro-2-methylpyrimidin-4-yl)thiazol-2-amine

https://huagongshe.com/reaction/1685292

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-AminothiazoleHCID 2155—
반응물4,6-Dichloro-2-methylpyrimidineHCID 234997—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물N-(6-chloro-2-methylpyrimidin-4-yl)thiazol-2-amineHCID 5920047751.5%

반응 조건

온도0 °C

반응 단계

To a cool (0° C.), stirring suspension of 2-aminothiazole (3.05 g, 0.0305 mol), 4,6-dichloro-2-methylpyrimidine (5.84 g, 0.0358 mol) in THF (50 mL) was added dropwise over 10 minutes via addition funnel a solution of t-BuOK (40 mL, 30% wt in THF, 0.1069 mol). The reaction was allowed to slowly warm to room temperature overnight. To the reaction was added water (40 mL) and the resulting clear solution was extracted with chloroform and then chloroform/methanol (4:1). The combined extracts were concentrated to near dryness to give a precipitate. The solid was collected by filtration to give the title material (3.559 g) as a solid. The filtrate was concentrated to dryness and the resulting solid was dissolved in boiling methanol and allowed to precipitate overnight aided with the addition of some water. The solid was collected by filtration, washed with water and air dried to give the title material (1.451 g) as a solid. The aqueous layer from the extraction was acidified with 10% HCl and a precipitate was formed. The solid was collected by filtration, washed with water to give the title material (1.559 g) as a solid. The solids were combined to give the title material (6.569 g, 95%). 1H NMR (400 MHz, DMSO-d6) δ (ppm): 2.53 (3H, s), 6.90 (1H, s), 7.21 (1H, d, J=3.5 Hz), 7.46 (1H, d, J=3.5 Hz), 11.87 (1H, s). LC/MS (M+H)+: 227, 229. HPLC ret. time (Condition E): 1.427 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08148400B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-ae7a13355a4240baa53f9d7444165ff6
출처 메모uspto-grants-2012_04