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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337233Generated: October 28, 2026

Diisopropylethylamine → HCID 71632163, compound

https://huagongshe.com/reaction/337233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
Reactant4-(Bromomethyl)benzenesulfonyl chlorideHCID 2734409—
SolventDichloromethaneHCID 6344—
ProductHCID 71632163HCID 7163216370%

Reaction Steps

Diisopropylethylamine (0.99 ml, 5.6 mmol) was added in one portion to a stirred solution of piperidin-4-yl-carbamic acid tert-butyl ester (0.37 g, 1.85 mmol) in DCM (20 ml) at room temperature. To this mixture was added 4-bromomethyl-benzenesulfonyl chloride (0.5 g, 1.85 mmol) in one portion and the mixture was stirred at room temperature under a nitrogen atmosphere for 1 hour. After this time the mixture was diluted with DCM (50 ml) and washed sequentially with HCl (1M solution, 20 ml), NaOH (1M solution, 20 ml) and brine (20 ml). The organic layer was separated, dried (MgSO4), filtered and concentrated. The resulting solid was collected by filtration, washed with diethyl ether and dried under vacuum to give the title compound (0.56 g, 70% yield) as an off-white solid. Tr=2.12 min, m/z (ES+) (M+Na)+ 457.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889716B2
Source datasetuspto-grants-2014_11
ORD IDord-7c0a003d78464e2db36809a2d9d88e3c
Source noteuspto-grants-2014_11