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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545641Generated: October 28, 2026

Tetrahydrofuran → HCID 67188838, compound

https://huagongshe.com/reaction/545641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 67188470HCID 67188470—
ProductHCID 67188838HCID 67188838—

Reaction Steps

A solution of tert-butyl 4-(4-bromo-2-cyanophenylamino)piperidine-1-carboxylate (1.00 g, 3 mmol) in THF (10 ml, 123 mmol) under argon was added borane-tetrahydrofuran complex (8 ml, 8 mmol) and stirred at RT for 20 h. The reaction was cooled to 0° C. and quenched with MeOH. The mixture was further diluted with EtOAc and washed with saturated aqueous NaHCO3 and brine, then dried (MgSO4). Evaporation gave a relatively pure crop of the desired product, tert-butyl 4-(2-(aminomethyl)-4-bromophenylamino)piperidine-1-carboxylate, which was used directly in the next step without further purification. MS m/e 385.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935709B2
Source datasetuspto-grants-2011_05
ORD IDord-b0f2decdd279429a84e6ad0661a71423
Source noteuspto-grants-2011_05