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HRID 974562作成日:2026年10月25日

Triethylamine → N-(3-Methyl-2-butenyl)-3-[4-(trifluoromethyl)phenoxy]-1-azetidinecarboxamide

https://huagongshe.com/reaction/974562

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物2-Buten-1-amine, 3-methyl-HCID 166921—
反応物3-[4-(Trifluoromethyl)phenoxy]azetidine oxalateHCID 12812500—
溶媒DichloromethaneHCID 6344—
生成物N-(3-Methyl-2-butenyl)-3-[4-(trifluoromethyl)phenoxy]-1-azetidinecarboxamideHCID 1505342783.8%

反応手順

A solution of 3.6 g. (0.022 mole) of 1,1'-carbonyldiimidazole in 100 ml of methylene chloride was cooled in a tap water bath and while stirring under nitrogen, 1.87 g (0.022 mole) of 3-methyl-2-butenylamine was added dropwise. After stirring for 1 hr, 6.2 g (0.02 mole) of 3-[4-(trifluoromethyl)phenoxy]azetidine oxalate was added all at once followed in 0.5 hr with 5 ml of triethylamine and stirring continued for an additional 16 hr. The reaction mixture was washed with 2×50 ml of water, dried over magnesium sulfate and concentrated on a rotary evaporator to yield a semi-solid residue. Trituration with isopropyl ether and filtration yielded 7 g of crude product which was recrystallized from ethanol-water to give 5.5 g (83.8%) of white crystals, m.p. 156.5°-158° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05068231
出典データセットuspto-grants-1991_11
ORD IDord-fe29ebebc93741e390c925f601b150df
出典メモuspto-grants-1991_11