Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171832Generated: November 1, 2026

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

https://huagongshe.com/reaction/1171832

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 μL g, 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 numberUS07829583B2
Source datasetuspto-grants-2010_11
ORD IDord-0532b3520fa44f36b052f7f30efb4a22
Source noteuspto-grants-2010_11