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HRID 326328作成日:2026年10月24日

Triethylamine → Methyl 2-chloro-5-[(6-methyl-2,3-dihydro-1,4-oxathiine-5-carbonyl)amino]benzoate

https://huagongshe.com/ja/reaction/326328

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Thionyl ChlorideHCID 24386—
反応物2-Methyl-5,6-dihydro-1,4-oxathiine-3-carboxylic acidHCID 539946—
反応物Methyl 5-Amino-2-chlorobenzoateHCID 5200412—
溶媒DichloromethaneHCID 6344—
生成物Methyl 2-chloro-5-[(6-methyl-2,3-dihydro-1,4-oxathiine-5-carbonyl)amino]benzoateHCID 46580892.7%

反応手順

Thionyl chloride (4.1 g, 0.034 mole) was added to a stirred mixture of 5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxylic acid (4.3 g, 0.027 mole) and methylene chloride (35 ml). The mixture was warmed to a gentle reflux for about 3.5 hours, left stirring overnight at room temperature, and then evaporated under reduced pressure. The solid residue, crude 5,6-dihydro-2-methyl-1,4-oxathiin-3-carbonyl chloride, was dissolved in methylene chloride (50 ml) and the solution treated dropwise at 5°-10° C. over 2 hours with a solution of methyl 5-amino-2-chlorobenzoate (5.1 g, 0.027 mole) and triethylamine (3.1 g, 0.031 mole) in methylene chloride (35 ml). The reaction mixture was stirred at room temperature for a further 3 hours and worked up by washing in sequence with water (50 ml), dilute hydrochloric acid (3.5%, 50 ml), water (50 ml), dilute sodium hydroxide (2%, 25 ml) and water (50 ml). The methylene chloride was then evaporated to leave an oil (8.2 g), which slowly solidified. Recrystallization from methanol (75 ml) gave a beige solid, m.p. 115°-117° C. (5.5 g, 62.5% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05268389
出典データセットuspto-grants-1993_12
ORD IDord-e8dabe3b24a44ebd97e0ab3560ef570b
出典メモuspto-grants-1993_12