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HRID 2238398作成日:2026年10月27日

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

https://huagongshe.com/reaction/2238398

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物TriethylamineHCID 8471—
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物Sodium BicarbonateHCID 516892—
反応物6-(Methoxycarbonyl)naphthalene-2-carboxylic acidHCID 3380217—
生成物Methyl 6-[(tert-butoxycarbonyl)amino]-2-naphthoateHCID 4454953278%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07718688B2
出典データセットuspto-grants-2010_05
ORD IDord-bd1c72b315d944a6b7df28551dc9fefd
出典メモuspto-grants-2010_05