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HRID 20179作成日:2026年10月23日

2,3-Difluorobenzaldehyde → tert-Butyl 1-(2,3-difluorobenzyl)-5-oxo-4-(2,2,2-trifluoroethyl)-1,4-diazepan-6-ylcarbamate

https://huagongshe.com/ja/reaction/20179

反応式

関与物質

役割名称HCID仕込み量
反応物2,3-DifluorobenzaldehydeHCID 137664—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物tert-Butyl 7-oxo-1-(2,2,2-trifluoroethyl)-1,4-diazepan-6-ylcarbamateHCID 66939478—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
生成物tert-Butyl 1-(2,3-difluorobenzyl)-5-oxo-4-(2,2,2-trifluoroethyl)-1,4-diazepan-6-ylcarbamateHCID 6843300788.6%

反応手順

A mixture of tert-butyl 7-oxo-1-(2,2,2-trifluoroethyl)-1,4-diazepan-6-ylcarbamate (51 mg, 0.16 mmol), 2,3-difluorobenzaldehyde (0.053 mL, 0.49 mmol), and sodium cyanoborohydride (31 mg, 0.49 mmol) in methanol (5 mL) was adjusted to pH 4 with acetic acid. After 0.5 h, saturated aqueous sodium bicarbonate was added and the mixture was extracted with dichloromethane (3×). The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated. Purification by silica gel chromatography [100% dichloromethane→95% dichloromethane/5% (10% ammonium hydroxide/methanol)] gave the title compound (62 mg). MS 438 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745427B2
出典データセットuspto-grants-2010_06
ORD IDord-01f51043ad52477d81f45ae29ff9fad2
出典メモuspto-grants-2010_06