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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786812Generated: October 30, 2026

N-(tert-Butoxycarbonyl)-1,5-diaminopentane → Tert-butyl (5-((2-chloroethyl)sulfonamido)pentyl)carbamate

https://huagongshe.com/reaction/1786812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(tert-Butoxycarbonyl)-1,5-diaminopentaneHCID 4352—
ReactantTriethylamineHCID 8471—
ReactantEthanesulfonylchloride, 2-chloro-HCID 15385—
SolventDichloromethaneHCID 6344—
ProductTert-butyl (5-((2-chloroethyl)sulfonamido)pentyl)carbamateHCID 86594118100%

Reaction Steps

To a stirred solution of 5-(tert-butoxycarbonylamino)pentylamine (1.00 g, 4.94 mmol) and triethylamine (689 μg, 4.94 mmol) in dichloromethane (22 mL) at 0° C. was added 2-chloro-1-ethanesulfonyl chloride (470 μL, 4.50 mmol). The reaction mixture was stirred for 2 h at room temperature and then washed with saturated aqueous sodium bicarbonate solution (15 mL). The organic layer was dried (Na2SO4) and the solvent was removed under reduced pressure to give the title compound (100% yield), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507751B2
Source datasetuspto-grants-2009_03
ORD IDord-13c5c19cd9ac4ba18e656885e01f98a7
Source noteuspto-grants-2009_03