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HRID 132443作成日:2026年10月27日

Methanol → (R)-3-(7-chloro-4-(hydroxymethyl)-1H-indazol-5-yl)-1-methoxy-1-oxopropan-2-yl benzoate

https://huagongshe.com/reaction/132443

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物ChloroformHCID 6212—
反応物Methanol, magnesium salt (2:1)HCID 164537—
反応物(R)-3-(4-(acetoxymethyl)-7-chloro-1H-indazol-5-yl)-1-methoxy-1-oxopropan-2-yl benzoateHCID 59732064—
生成物(R)-3-(7-chloro-4-(hydroxymethyl)-1H-indazol-5-yl)-1-methoxy-1-oxopropan-2-yl benzoateHCID 5973206267%

反応手順

(R)-3-(4-(acetoxymethyl)-7-chloro-1H-indazol-5-yl)-1-methoxy-1-oxopropan-2-yl benzoate (8.5g, 19.73 mmol) in a mixture of chloroform (80.0 ml, 992 mmol) and methanol (60.0 ml, 1483 mmol) was added magnesium methoxide (4.18 ml, 39.5 mmol). After 3 h, quenched with 1.0 M HCl and extracted with dichloromethane (300 mL). The crude product was purified by flash chromatography using 70% EtOAc in hexane to give (R)-3-(7-chloro-4-(hydroxymethyl)-1H-indazol-5-yl)-1-methoxy-1-oxopropan-2-yl benzoate in 67% yield. 1H NMR (500 MHz, CDCl3): in δ 8.09 (s, 1H), 7.93 (d, J=7.5 Hz, 1H), 7.47 (m, 1H), 7.32 (t, J=8 Hz, 2H), 7.22 (s, 1H), 5.49 (m, 1H), 4.99 (m, 2H), 3.45-3.41 (m, 1H), 3.68 (s, 3H), 3.36-3.31 (m, 1H); MS (ESI) 389 (M+H); Rf=2.07.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384931B2
出典データセットuspto-grants-2008_06
ORD IDord-cd3f5188bd7d4314b3f438c5af0538c8
出典メモuspto-grants-2008_06