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HRID 14448Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/14448

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-(tert-Butoxycarbonyl)-1,5-diaminopentaneHCID 4352—
EduktTriethylamineHCID 8471—
EduktEthanesulfonylchloride, 2-chloro-HCID 15385—
LösungsmittelDichloromethaneHCID 6344—
ProduktTert-butyl (5-((2-chloroethyl)sulfonamido)pentyl)carbamateHCID 86594118100%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732441B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-617ecb4a7d1545669dc6487048b896de
Quellennotizuspto-grants-2010_06