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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 885494Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/885494

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
PatentnummerUS08242135B2
Quelldatensatzuspto-grants-2012_08
ORD IDord-f94f1ff505394c20ae8c0967476c6257
Quellennotizuspto-grants-2012_08