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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177478Generated: October 31, 2026

Sodium borohydride → HCID 44601272, compound

https://huagongshe.com/reaction/1177478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-Fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)benzaldehydeHCID 59174907—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 44601272HCID 44601272—

Reaction Steps

To a solution at 0° C. of 3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine-2-yl)benzaldehyde (2.00 g, 5.34 mmol) in THF (50 mL) and MeOH (25 mL) was added sodium borohydride (0.188 mL, 5.34 mmol). The reaction mixture was allowed to warm up to ambient temperature. The crude reaction mixture, after 1 h, was concentrated in vacuo and purified by silica gel chromatography to afford (3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine-2-yl)phenyl)methanol. MS (ESI) m/z: calculated: 376.1: Observed: 377.0 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842685B2
Source datasetuspto-grants-2010_11
ORD IDord-ce4a0e0a5c64401b8ba2ab7f817c0457
Source noteuspto-grants-2010_11