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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2238398생성일: 2026년 10월 26일

tert-Butanol → Methyl 6-[(tert-butoxycarbonyl)amino]-2-naphthoate

https://huagongshe.com/reaction/2238398

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물TriethylamineHCID 8471—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물Sodium BicarbonateHCID 516892—
반응물6-(Methoxycarbonyl)naphthalene-2-carboxylic acidHCID 3380217—
생성물Methyl 6-[(tert-butoxycarbonyl)amino]-2-naphthoateHCID 4454953278%

반응 단계

A suspension of 6-(methoxycarbonyl)-2-naphthoic acid [J. Med. Chem., 2004, 47, 303-324] (146) (1.21 g, 5.26 mmol) in dry t-BuOH (20 mL) containing powdered molecular sieves (1 g) was treated with Et3N (0.88 mL, 6.31 mmol) and stud under N2 at room temperature for 30 min. DPPA (1.25 mL, 5.80 mmol) was added and the mixture was sired at reflux for 7 h, then cooled and poured into dilute aqueous NaHCO3. The resting solid was purified by chromatography on silica gel, eluting with CH2Cl2, followed by trituration with iPr2O and recrystallization from EtOAc to give methyl 6-[(tert-butoxycarbonyl)amino]-2-naphthoate (147) (1.24 g, 78%) as a white solid: mp 178-180° C.; 1H NMR [(CD3)2SO] δ 9.76 (s, 1H), 8.51 (s, 1H), 8.19 (s, 1H), 8.02 (d, J=9.0 Hz, 1H), 7.90 (dd, J=8.6, 1.6 Hz, 1H), 7.86 (d, J=8.7 Hz, 1H), 7.59 (dd, J=8.9, 2.1 Hz, 1H), 3.89 (s, 3H), 1.52 (s, 9H). Anal. (C17H19NO4) C, H, N.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07718688B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-bd1c72b315d944a6b7df28551dc9fefd
출처 메모uspto-grants-2010_05