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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17318생성일: 2026년 10월 23일

Dimethyl Sulfoxide → 2-[2-(Benzyloxy)-1,1-dimethylethyl]-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile

https://huagongshe.com/ko/reaction/17318

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물TriethylamineHCID 8471—
반응물(3S)-(-)-3-(Dimethylamino)pyrrolidineHCID 7019156—
반응물2-(2-Benzyloxy-1,1-dimethylethyl)-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrileHCID 68584461—
용매Ethyl AcetateHCID 8857—
생성물2-[2-(Benzyloxy)-1,1-dimethylethyl]-7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrileHCID 6858600691.1%

반응 조건

온도90 °C

반응 단계

Triethylamine (222 μl, 1.59 mmol), (3S)-3-(dimethylamino)pyrrolidine (152 μl, 1.19 mmol) were added to a dimethyl sulfoxide (16.5 ml) solution of 2-[2-(benzyloxy)-1,1-dimethylethyl]-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile (I-66) (330 mg, 0.796 mmol), followed by stirring overnight at 90° C. After cooling, the reaction liquid was diluted with ethyl acetate, washed three times with saturated brine, then dried over anhydrous magnesium sulfate, concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (chloroform:methanol=100:1) to obtain the entitled compound (369 mg, 91%) as a pale brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737166B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-4bf106d9387a4d12a650fb0b39fbb4e9
출처 메모uspto-grants-2010_06