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HRID 10341作成日:2026年10月24日

Water → 5,6-Difluoro-2-methyl-1,2,3,4-tetrahydro-quinoline-8-carboxylic acid methyl ester

https://huagongshe.com/ja/reaction/10341

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物5,6-Difluoro-2-methylquinoline-8-carboxylic acid methyl esterHCID 21041191—
反応物HCID 178418361HCID 178418361—
触媒PlatinumHCID 23939—
溶媒Acetic AcidHCID 176—
生成物5,6-Difluoro-2-methyl-1,2,3,4-tetrahydro-quinoline-8-carboxylic acid methyl esterHCID 2104119068.9%

反応手順

A solution of 8.0 g (33.7 mmol) of 5,6-difluoro-2-methylquinoline-8-carboxylic acid methyl ester (Example 33) in 100 mL of glacial acetic acid is treated with 2.15 g of platinum on carbon (0.8 g of active catalyst+62.8% water) and then shaken in a hydrogen atmosphere at temperatures of 24° C. to 29° C. and pressures of 23.9 to 46.6 psi for 3 hours. The catalyst is removed by filtration and the solvent is removed in vacuo at 50° C. The residue is triturated with water (50 mL) and extracted with dichloromethane (2×200 mL). The combined organic layers are stirred with 5% sodium bicarbonate solution, washed with water, dried (MgSO4), filtered and evaporated in vacuo. The residue is chromatographed over flash grade silica gel (230–400 mesh) eluting with dichloromethane to give 5.6 g of the title compound as a light yellow oil. 1H NMR (400 MHz, CDCl3): 7.66 (bs, 1H), 7.49 (m, 1H), 3.82 (s, 3H), 3.46 (m, 1H), 2.88 (m, 1H), 2.67 (m, 1H), 1.97 (m, 1H), 1.27 (d, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094780B1
出典データセットuspto-grants-2006_08
ORD IDord-cf7993e3573e421a894de7cb83cffe3e
出典メモuspto-grants-2006_08