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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773601Generated: November 1, 2026

Sodium borohydride → HCID 58056216, compound

https://huagongshe.com/reaction/1773601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58056153HCID 58056153—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58056216HCID 58056216—

Reaction Steps

Sodium borohydride (30 mg, 0.079 mmol) was added to a solution of 6-formyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid {2-[4-(tert-butyl-dimethyl-silanyloxy)-cyclohexyloxy]-5-chloro-phenyl}-amide (20 mg, 0.038 mmol) in a mixture of tetrahydrofuran (1.5 mL) and water (0.1 mL) and the resulting mixture was stirred at room temperature for 2.5 hours. The solvent was evaporated under reduced pressure to give 6-hydroxymethyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid {2-[4-(tert-butyl-dimethyl-silanyloxy)-cyclohexyloxy]-5-chloro-phenyl}-amide as an oily residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255110B2
Source datasetuspto-grants-2016_02
ORD IDord-d31973c3925145c2b4e03ed1c379178f
Source noteuspto-grants-2016_02