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HRID 1294824作成日:2026年10月26日

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

https://huagongshe.com/reaction/1294824

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物3-Isoxazolamine, 5-(1,1-dimethylethyl)-, hydrochloride (1:1)HCID 11969519—
反応物2-Tert-butoxycarbonylamino-pentanoic acid methyl esterHCID 23278200—
溶媒TetrahydrofuranHCID 8028—
生成物[1-(5-Tert-butyl-isoxazol-3-ylcarbamoyl)butyl]-carbamic acid tert-butyl esterHCID 69419406141.2%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07241786B2
出典データセットuspto-grants-2007_07
ORD IDord-9c63790266c841a5a98ec1b18deb6e63
出典メモuspto-grants-2007_07