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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1294824생성일: 2026년 10월 26일

Toluene → [1-(5-Tert-butyl-isoxazol-3-ylcarbamoyl)butyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1294824

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물3-Isoxazolamine, 5-(1,1-dimethylethyl)-, hydrochloride (1:1)HCID 11969519—
반응물2-Tert-butoxycarbonylamino-pentanoic acid methyl esterHCID 23278200—
용매TetrahydrofuranHCID 8028—
생성물[1-(5-Tert-butyl-isoxazol-3-ylcarbamoyl)butyl]-carbamic acid tert-butyl esterHCID 69419406141.2%

반응 단계

To a solution of 5-tert-butyl-isoxazol-3-ylamine hydrochloride (1.22 g, 8.69 mmol) in THF was added 2 M AIMe3 in toluene (4.3 ml, 8.6 mmol) at room temperature and stirred for 1 hr. A solution of 2-tert-butoxycarbonylamino-pentanoic acid methyl ester (1.005 g, 4.34 mmol) in THF was added and the resulting mixture was stirred at room temperature over the weekend. The mixture was quenched with Rochelle salt and extracted with ethyl acetate. The organic layer was separated, dried and concentrated to give 2.08 g of the title compound as a crude oil. The oil was purified by silica gel column chromatography using 1% methanl in methylenechloride as eluent to give the title compound as a white solid (0.554 g). 1H NMR (CDCl3) □ 8.8 (brs, 1H), 6.7 (s, 1H), 4.85 (brs, 1H), 4.22 (m, 1H), 1.9 (m, 1H), 1.4-1.7 (m, 3H), 1.45 (s, 9H), 1.44 (s, 9H), 0.97 (t, 3H) ppm. LC-MS M+1=340.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07241786B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-9c63790266c841a5a98ec1b18deb6e63
출처 메모uspto-grants-2007_07