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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2204825생성일: 2026년 10월 25일

Water → 4-(5-(Bis(tert-butoxycarbonyl)amino)-6-(3-phenylisoxazol-5-yl)pyrazin-2-yl)benzoic acid

https://huagongshe.com/reaction/2204825

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium CarbonateHCID 10340—
반응물4-Carboxyphenylboronic AcidHCID 312183—
반응물tert-butyl (5-bromo-3-(3-phenylisoxazol-5-yl)pyrazin-2-yl)-N-tert-butoxycarbonyl-carbamateHCID 59472363—
촉매HCID 178418397HCID 178418397—
용매AcetonitrileHCID 6342—
생성물4-(5-(Bis(tert-butoxycarbonyl)amino)-6-(3-phenylisoxazol-5-yl)pyrazin-2-yl)benzoic acidHCID 5947241199%

반응 조건

온도110 °C

반응 단계

Tert-butyl N-[5-bromo-3-(3-phenylisoxazol-5-yl)pyrazin-2-yl]-N-tert-butoxycarbonyl-carbamate (184 mg, 0.3379 mmol), 4-boronobenzoic acid (56.07 mg, 0.3379 mmol) and Na2CO3 (71.63 mg, 0.6758 mmol) were suspended in MeCN (2.896 mL)/water (2.896 mL) and the mixture de-gassed (×5) and treated with Pd(PPh3)4 (39.05 mg, 0.03379 mmol). The reaction was de-gassed again and heated at 110° C. in the microwave for 30 minutes. The reaction mixture was concentrated to half its original volume and washed with DCM. The aqueous phase was acidified to pH4 by (2M HCl) and resulting precipitate collected, washed with water and dried under vacuum (120 mg, 99% Yield). MS (ES+) 359.12

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09365557B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-6cb34d3084a74dc2ba616fd9510333ca
출처 메모uspto-grants-2016_06