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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 527552생성일: 2026년 10월 24일

Ammonium Chloride → 2-[(3,3-Dimethyl-2,3-dihydro-1-benzofuran-4-yl)oxy]-5-pyrimidinamine

https://huagongshe.com/ko/reaction/527552

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물2-[(3,3-Dimethyl-2,3-dihydro-1-benzofuran-4-yl)oxy]-5-nitropyrimidineHCID 67958694—
촉매IronHCID 23925—
용매Oxolane--water (1/1)HCID 21881883—
생성물2-[(3,3-Dimethyl-2,3-dihydro-1-benzofuran-4-yl)oxy]-5-pyrimidinamineHCID 6795852368.2%

반응 단계

To a solution of 2-[(3,3-dimethyl-2,3-dihydro-1-benzofuran-4-yl)oxy]-5-nitropyrimidine (Intermediate 64, 1.257 g) in a mixture tetrahydrofuran/water (30 ml/15.00 ml) iron (1.222 g, 21.88 mmol) and ammonium chloride (1.170 g, 21.88 mmol) were added. The reaction mixture was stirred at room temperature for 48 hours. The catalyst was filtered off, and the filtrate was extracted with ethyl acetate (3×50 ml). The combined organic layers were dried over sodium sulphate, filtered and evaporated. The residue was recrystallized from ethyl acetate to afford the title compound (768 mg) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346790B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-bf817dcfa925476692a0d8586b6d5c05
출처 메모uspto-grants-2016_05