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HRID 502544생성일: 2026년 10월 27일

Triethylamine → Tert-butyl 3-(2-(benzo[d]isothiazol-3-ylamino)ethylcarbamoyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/502544

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-((Tert-butoxy)carbonyl)piperidine-3-carboxylic acidHCID 2735647—
반응물N1-(benzo[d]isothiazol-3-yl)ethane-1,2-diamineHCID 16768374—
용매DichloromethaneHCID 6344—
생성물Tert-butyl 3-(2-(benzo[d]isothiazol-3-ylamino)ethylcarbamoyl)piperidine-1-carboxylateHCID 11854495—

반응 단계

A mixture of N1-(benzo[d]isothiazol-3-yl)ethane-1,2-diamine (600 mg, 3.11 mmol), 1-(tert-butoxycarbonyl)piperidine-3-carboxylic acid (854 mg, 3.7 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (585 mg, 3.7 mmol) and triethylamine (577 μL, 3.7 mmol) in dichloromethane (40 mL) was allowed to stir at room temperature overnight. The reaction mixture was washed successively with 1N aqueous hydrochloric acid, saturated sodium bicarbonate solution and water, then dried over anhydrous sodium sulfate, filtered and the filtrate concentrated under reduced pressure. Purification by flash column chromatography, on silica gel, eluting with a mixture of 25% ethyl acetate in hexanes gave fractions that were combined and concentrated under reduced pressure to yield tert-butyl 3-(2-(benzo[d]isothiazol-3-ylamino)ethylcarbamoyl)piperidine-1-carboxylate as a white solid, (325 mg). 1H NMR (300 MHz, DMSO-d6): 8.1 (m, 2H), 7.92 (m, 3H), 7.9 (d, 1H), 7.5 (m, 1H), 7.3 (m, 1H), 3.9 (m, 2H), 3.5 (m, 2H), 3.3 (m, 2H), 2.8 (m, 2H), 2.2 (m, 1H), 1.8 (m, 1H), 1.6 (m, 3H), 1.3 ppm (s, 9H). MW=405 confirmed by LC-MS, tr=3.81 min (Method B) MH+=406.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07776847B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-5e4034dc2ee34719adfc155f90dd7663
출처 메모uspto-grants-2010_08