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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850121Generated: October 30, 2026

Sodium triacetoxyborohydride → (S)-tert-butyl 1-(3-fluoro-4-((3,3,4-trimethylpiperazin-1-yl)methyl)phenyl)ethylcarbamate

https://huagongshe.com/reaction/1850121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantDichloromethane methanolHCID 21226129—
Reactant1,2,2-Trimethylpiperazine dihydrochlorideHCID 23289382—
Reactant(S)-tert-butyl 1-(3-fluoro-4-formylphenyl)ethylcarbamateHCID 86730149—
SolventTetrahydrofuranHCID 8028—
Product(S)-tert-butyl 1-(3-fluoro-4-((3,3,4-trimethylpiperazin-1-yl)methyl)phenyl)ethylcarbamateHCID 8673015149%

Reaction Steps

A solution of (S)-tert-butyl 1-(3-fluoro-4-formylphenyl)ethylcarbamate (267 mg, 1 mmol) and 1,2,2-trimethylpiperazine dihydrochloride (402 mg, 2 mmol) in THF (5 mL) was stirred at room temperature for 1 h and treated with sodium triacetoxyborohydride (848 mg, 4 mmol). The resulting mixture was stirred at room temperature for 16 h. The reaction mixture was quenched with saturated aqueous solution of NaHCO3 (15 mL) and extracted with EtOAc (3×25 mL). Combined organics were dried over Na2SO4, filtered and concentrated. Silica gel column chromatography (MeOH/CH2Cl2 0 to 10%) provided (S)-tert-butyl 1-(3-fluoro-4-((3,3,4-trimethylpiperazin-1-yl)methyl)phenyl)ethylcarbamate as a white solid (186 mg, 49% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957068B2
Source datasetuspto-grants-2015_02
ORD IDord-ad08149ac2e040339b3d30da4167fdc3
Source noteuspto-grants-2015_02