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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180182Generated: October 30, 2026

Sodium borohydride → HCID 68532412, compound

https://huagongshe.com/reaction/2180182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22490346HCID 22490346—
ReactantHCID 22490374HCID 22490374—
SolventMethanolHCID 887—
ProductHCID 68532412HCID 6853241280.6%

Reaction Steps

To a stirred solution of (3,4-difluorophenyl)-(2-oxo-ethyl)-carbamic acid-tert-butyl ester (1.23 g, 4.3 mmol) in MeOH (35 mL) under Ar at room temperature was added a solution of C-[4-(4-iodo-phenyl)-1-methyl-piperidin-4-yl]-methylamine (1.49 g, 4.5 mmol, 1.05 eq.) in MeOH (10 mL). The mixture was stirred at room temperature for 5 h then NaBH4 (0.255 g, 6.75 mmol, 1.5 eq) was added and the resulting mixture was stirred for a further 1 h and then was quenched by the addition of 1N aqueous NaOH (40 mL). The mixture was extracted twice with Et2O (2×50 mL) and the combined organic extracts were washed with saturated brine (100 mL) and dried over Na2SO4. Filtration and concentration of the filtrate by rotary evaporation gave the crude product which was purified by flash column chromatography by eluting with 12% EtOAc/hexanes to give (3,4-difluoro-phenyl)-(2-{[4-(4-iodo-phenyl)-1-methyl-piperidin-4-ylmethyl]-amino}-ethyl)-carbamic acid tert-butyl ester (2.03 g, 76%) as a pale oil. MS (ESI): 585.9/587.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06887889B2
Source datasetuspto-grants-2005_05
ORD IDord-665f6e2d88714b22bce26db8c3624bdb
Source noteuspto-grants-2005_05