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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174655Generated: November 1, 2026

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

https://huagongshe.com/reaction/1174655

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 numberUS07838535B2
Source datasetuspto-grants-2010_11
ORD IDord-ad0c9041562f4c3a9ba23c7f7581a97f
Source noteuspto-grants-2010_11