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HRID 133135作成日:2026年10月26日

1,2-Dichloroethane → tert-Butyl (6S,9R)-6-(2,3-difluorophenyl)-3-(2,2,2-trifluoroethyl)-6,7,8,9-tetrahydro-5H-[1,2,4]triazolo[4,3-a]azepin-9-ylcarbamate

https://huagongshe.com/reaction/133135

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物TriethylamineHCID 8471—
反応物HOAtHCID 181649—
反応物Sodium BicarbonateHCID 516892—
反応物3,3,3-Trifluoropropionic acidHCID 2777972—
反応物HCID 178453872HCID 178453872—
溶媒DichloromethaneHCID 6344—
生成物tert-Butyl (6S,9R)-6-(2,3-difluorophenyl)-3-(2,2,2-trifluoroethyl)-6,7,8,9-tetrahydro-5H-[1,2,4]triazolo[4,3-a]azepin-9-ylcarbamateHCID 59734931—

反応手順

Triethylamine (0.259 mL, 1.86 mmol) was added to a solution of tert-butyl (3R,6S)-6-(2,3-difluorophenyl)-2-hydrazonoazepan-3-ylcarbamate from Step A (548 mg, 1.55 mmol), 3,3,3-trifluoropropionic acid (0.205 mL, 2.32 mmol), EDC (356 mg, 1.86 mmol), and 1-hydroxy-7-azabenzotriazole (253 mg, 1.86 mmol) in dichloromethane (55 mL). After 18 h, saturated aqueous NaHCO3 was added and the mixture was extracted with CH2Cl2 (3×). The combined organic extracts were dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH—100:0 to 96:4, to give the title compound. MS: m/z=447 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390798B2
出典データセットuspto-grants-2008_06
ORD IDord-322f995a0886448891d21536f696947a
出典メモuspto-grants-2008_06