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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 872745생성일: 2026년 10월 25일

5-tert-Butyl-1,2-oxazole-3-carboxylic acid → (S)-5-tert-butyl-N-(1-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)isoxazole-3-carboxamide

https://huagongshe.com/reaction/872745

반응식

참여 물질

역할이름HCID투입량
반응물5-tert-Butyl-1,2-oxazole-3-carboxylic acidHCID 17389664—
반응물(S)-4-(1-(2-aminopropyl)-1H-pyrazol-3-yl)-2-chlorobenzonitrileHCID 67170882—
생성물(S)-5-tert-butyl-N-(1-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)isoxazole-3-carboxamideHCID 7065580853.6%

반응 단계

(S)-5-tert-butyl-N-(1-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)isoxazole-3-carboxamide was prepared using the method of Example 34(d) starting from (S)-4-(1-(2-aminopropyl)-1H-pyrazol-3-yl)-2-chlorobenzonitrile (200 mg, 0.69 mmol) and 5-tert-butylisoxazole-3-carboxylic acid (132 mg, 0.782 mmol). The product was purified by Flash-chromatography (reverse phase). Yield 53.6%. 1H-NMR (400 MHz; MeOD): δ 1.26 (d, 3H), 1.35 (s, 9H), 4.26-4.45 (m, 2H), 4.51-4.63 (m, 1H), 6.34 (s, 1H), 6.77 (d, 1H), 7.70 (d, 1H), 7.77 (dd, 1H), 7.87 (dd, 1H), 8.09 (dd, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08975254B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-40bdaba3e821435e9707207ebd5788e3
출처 메모uspto-grants-2015_03