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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 872736생성일: 2026년 10월 24일

5-(Hydroxymethyl)-1,2-oxazole-3-carboxylic acid → HCID 70657098, 화합물

https://huagongshe.com/ko/reaction/872736

반응식

참여 물질

역할이름HCID투입량
반응물5-(Hydroxymethyl)-1,2-oxazole-3-carboxylic acidHCID 8027249—
반응물(S)-4-(1-(2-aminopropyl)-1H-pyrazol-3-yl)-2-chlorobenzonitrileHCID 67170882—
생성물HCID 70657098HCID 706570981.9%

반응 단계

(S)—N-(1-(3-(3-chloro-4-cyanophenyl)-1H-pyrazol-1-yl)propan-2-yl)-5-(hydroxymethyl)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, 0.675 mmol) and 5-(hydroxymethyl)isoxazole-3-carboxylic acid (126 mg, 0.878 mmol). The product purified twice by Flash-chromatography (normal phase and reverse phase) and triturated using diethyl ether. Yield 1.9%. 1H-NMR (400 MHz; MeOD): δ 1.26 (d, 3H), 4.28-4-43 (m, 2H), 4.52-4.63 (m, 1H), 4.68 (d, 2H), 6.57 (t, 1H), 6.77 (d, 1H), 7.70 (d, 1H), 7.78 (dd, 1H), 7.88 (dd, 1H), 8.07 (dd, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08975254B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-13897a7d6b1240fe9d8e07921cce7472
출처 메모uspto-grants-2015_03