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HRID 228037作成日:2026年10月26日

Citric Acid → 4-tert-butoxycarbonylamino-N-(4-chlorophenyl)-N-methylbicyclo[2.2.2]octane-1-carboxamide

https://huagongshe.com/reaction/228037

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物TrichloroacetonitrileHCID 11011—
反応物TriphenylphosphineHCID 11776—
反応物4-Chloro-N-methylbenzenamineHCID 70272—
反応物4-{[(Tert-butoxy)carbonyl]amino}bicyclo[2.2.2]octane-1-carboxylic acidHCID 23150738—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物4-tert-butoxycarbonylamino-N-(4-chlorophenyl)-N-methylbicyclo[2.2.2]octane-1-carboxamideHCID 23150517—

反応手順

4-tert-Butoxycarbonylaminobicyclo[2.2.2]octane-1-carboxylic acid (101 mg) was dissolved in dichloromethane (2 mL). To this solution, trichloroacetonitrile (74.0 μL) and triphenylphosphine (196 mg) in dichloromethane (1.5 mL) were sequentially added and the mixture was stirred at room temperature for 2 hours. This was followed by addition of triethylamine (0.18 mL) and 4-chloro-N-methylaniline (98.6 μL) and stirring at room temperature for additional 5.5 hours. The reaction mixture was then poured into aqueous citric acid (5 mL) and was extracted with ethyl acetate (3×10 mL). The ethyl acetate extracts were combined, washed with saturated aqueous sodium bicarbonate solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by a silica gel column (eluant:hexane:ethyl acetate=2:1) to give 4-tert-butoxycarbonylamino-N-(4-chlorophenyl)-N-methylbicyclo[2.2.2]octane-1-carboxamide (91.4 mg) as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560569B2
出典データセットuspto-grants-2009_07
ORD IDord-3233b079ee80401286c5780430e054a0
出典メモuspto-grants-2009_07