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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270955Generated: October 30, 2026

Sodium borohydride → HCID 15958148, compound

https://huagongshe.com/reaction/270955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 15958110HCID 15958110—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15958148HCID 1595814847%

Reaction Steps

To a stirred solution of 4.4 mg (0.115 mmol) of sodium borohydride (NaBH4) in 2 mL of methanol (MeOH) was added a solution of 35 mg (0.104 mmol) of 6-(4-benzyloxy-phenyl)-7-cyclohexyl-pyrazolo[1,5-a]pyrimidine-3-carbaldehyde in 3 mL of tetrahydrofuran (THF) and the resulting mixture was stirred at rt for 30 min when analysis by TLC indicated complete conversion of starting material to product. The reaction mixture was quenched by the addition of saturated ammonium chloride solution, and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over sodium sulfate and evaporated to give (after lyophilization) 20 mg (47% yield) of [6-(4-benzyloxy-phenyl)-7-cyclohexyl-pyrazolo[1,5-a]pyrimidin-3-yl]-methanol (479) as a white solid (85% purity) as indicated by 1H NMR (containing small traces of starting material); LC-MS—calcd for C26H27N3O2 [M++H]+: 414.21, found: 414.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449488B2
Source datasetuspto-grants-2008_11
ORD IDord-ace0e07fe80c48bf8ece5696a7bea962
Source noteuspto-grants-2008_11