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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41104생성일: 2026년 10월 23일

Acetic Acid → (R)-4-(1-((4-(tert-butoxycarbonyl)morpholin-2-yl)methyl)-5-methyl-1H-benzo[d]imidazol-2-yl)-3,5-difluorobenzoic acid

https://huagongshe.com/ko/reaction/41104

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물3,5-Difluoro-4-formylbenzoic acidHCID 45073629—
반응물(R)-tert-butyl 2-((2-amino-4-methylphenylamino)methyl)morpholine-4-carboxylateHCID 67170278—
용매MethanolHCID 887—
생성물(R)-4-(1-((4-(tert-butoxycarbonyl)morpholin-2-yl)methyl)-5-methyl-1H-benzo[d]imidazol-2-yl)-3,5-difluorobenzoic acidHCID 6716964282.3%

반응 단계

A mixture of (R)-tert-butyl 2-((2-amino-4-methylphenylamino)methyl)morpholine-4-carboxylate (600 mg, 1.87 mmol), 3,5-difluoro-4-formylbenzoic acid (347 mg, 1.87 mmol) and acetic acid (0.534 ml, 9.33 mmol) in methanol (15.0 ml) was stirred for 1.5 hr at room temperature. The mixture was then concentrated under reduced pressure, and the residue was purified by silica gel flash chromatography, eluting with mixtures of EtOAc and heptane, to afford (R)-4-(1-((4-(tert-butoxycarbonyl)morpholin-2-yl)methyl)-5-methyl-1H-benzo[d]imidazol-2-yl)-3,5-difluorobenzoic acid (750 mg, 82%) as an oil. The oil was analyzed on analytical HPLC MS using the high pH gradient method (mobile phase: 5-95% B; A: H2O with 10 mM NH4CO3 and 0.375% NH4OH v/v; B: CH3CN; 2.25 min run; X-Bridge C18; column size: 2.1×30 mm; particle size: 5 μm). MS m/z 488.4 [M+H]+ (ESI), Rt 1.56 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530467B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-36aa6bd91acc4a919a71b1846cced277
출처 메모uspto-grants-2013_09