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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41517생성일: 2026년 10월 24일

Methanol → 5-(2-Chloro-5-methylpyrimidin-4-ylamino)benzo[d]oxazol-2(3H)-one

https://huagongshe.com/ko/reaction/41517

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물5-Amino-2,3-dihydro-1,3-benzoxazol-2-oneHCID 26856—
반응물Pyrimidine, 2,4-dichloro-5-methyl-HCID 74508—
용매WaterHCID 962—
생성물5-(2-Chloro-5-methylpyrimidin-4-ylamino)benzo[d]oxazol-2(3H)-oneHCID 5807138771%

반응 단계

To a vial with 5-aminobenzo[d]oxazol-2(3H)-one (300.1 mg, 2.0 mmol) and 2,4-dichloro-5-methylpyrimidine (423.8 mg, 2.6 mmol), MeOH (8 mL) and H2O (2 mL) were added. The turbid mixture was stirred at room temperature for 64 h. Precipitate from reaction mixture was collected by filtration, washing with EtOAc (3 mL×2), and was further dried in vacuo. 5-(2-Chloro-5-methylpyrimidin-4-ylamino)benzo[d]oxazol-2(3H)-one was obtained as an off-white solid: 394 mg (71% yield); 1H NMR (300 MHz, DMSO) δ 11.68 (br s, 1H), 8.62 (s, 1H), 7.94 (d, J=0.8, 1H), 6.97 (d, J=2.0, 1H), 6.82 (d, J=8.1, 1H), 6.74 (dd, J=2.0, 8.1, 1H), 2.15 (s, 3H); LCMS (M+) m/z 277.10.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530656B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-7bf7f454a19f4f6f98ecb09d8f336a9f
출처 메모uspto-grants-2013_09