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HRID 14448作成日:2026年10月25日

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

https://huagongshe.com/reaction/14448

反応式

関与物質

役割名称HCID仕込み量
反応物N-(tert-Butoxycarbonyl)-1,5-diaminopentaneHCID 4352—
反応物TriethylamineHCID 8471—
反応物Ethanesulfonylchloride, 2-chloro-HCID 15385—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl (5-((2-chloroethyl)sulfonamido)pentyl)carbamateHCID 86594118100%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732441B2
出典データセットuspto-grants-2010_06
ORD IDord-617ecb4a7d1545669dc6487048b896de
出典メモuspto-grants-2010_06