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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402141Generated: October 27, 2026

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

https://huagongshe.com/reaction/1402141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium borohydrideHCID 4311764—
Reactantethyl 3-(5-amino-3-tert-butyl-1H-pyrazol-1-yl)benzoateHCID 21867322—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product[3-(5-Amino-3-tert-butyl-pyrazol-1-yl)-phenyl]-methanolHCID 2186731887%

Reaction Steps

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+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907094B2
Source datasetuspto-grants-2014_12
ORD IDord-3f684ee64dae47d8bbf3e55f319ff331
Source noteuspto-grants-2014_12