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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 630738생성일: 2026년 10월 26일

Triethylamine → [3-(5-Amino-3-tert-butyl-pyrazol-1-yl)-phenyl]-methanol

https://huagongshe.com/reaction/630738

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium borohydrideHCID 4311764—
반응물ethyl 3-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)benzoateHCID 21867322—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물[3-(5-Amino-3-tert-butyl-pyrazol-1-yl)-phenyl]-methanolHCID 2186731887%

반응 단계

To a solution of Intermediate 29a (1.00 g, 3.48 mmol) and Et3N (265 μL, 1.91 mmol) in EtOH (35 mL) was added NaBH4 (198 mg, 5.23 mmol) and the suspension stirred at RT for 1.5 h. NaBH4 (198 mg, 5.23 mmol) was added and the suspension stirred for a further 19 h. NaBH4 (1.31 g, 34.8 mmol) was added and the suspension stirred for a further 24 h, then diluted with water and extracted with DCM. The combined organics were dried and concentrated in vacuo. The residue was purified by FCC, using 0-10% [2M NH3 in MeOH] in DCM, to give the title compound as a white solid (740 mg, 87%). LCMS (Method 3): Rt 2.05 min, m/z 246 [MH+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09315503B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-43a0898a00d6435a80328f902108cfce
출처 메모uspto-grants-2016_04