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HRID 848141作成日:2026年10月27日

Benzyloxycarbonylglycine → Benzyl{[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]methyl}carbamate

https://huagongshe.com/reaction/848141

反応式

関与物質

役割名称HCID仕込み量
反応物BenzyloxycarbonylglycineHCID 14349—
反応物Thionyl ChlorideHCID 24386—
反応物2-Amino-2'-fluoro-5-nitrobenzophenoneHCID 67657—
溶媒TetrahydrofuranHCID 8028—
生成物Benzyl{[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]methyl}carbamateHCID 20562352—

反応手順

45 g of carbobenzoxy-glycine dissolved in 1 liter of absolute tetrahydrofuran are treated dropwise while cooling with ice with 20 ml of thionyl chloride and stirred for 1 hour while cooling with ice. There is then rapidly added dropwise thereto a suspension of 50 g of 2-amino-5-nitro-2'-fluorobenzophenone in 200 ml of absolute tetrahydrofuran and the mixture is stirred at room temperature for 18 hours. The solution obtained is concentrated and the residue is treated with ice and 10% sodium bicarbonate solution and extracted with methylene chloride. The organic solution is dried over sodium sulphate, filtered and concentrated. The residue is dissolved in a small amount of hot ethyl acetate, concentrated partially and treated with ether. Benzyl{[[2-(o-fluorobenzoyl)-4-nitrophenyl]carbamoyl]methyl}-carbamate is obtained. The mother liquors are purified on a 100 g silica gel column using methylene chloride as the eluting agent, an additional amount of the aforementioned product being obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04294758
出典データセットuspto-grants-1981_10
ORD IDord-473149f8530a4ff5aa4d9fb72addd08d
出典メモuspto-grants-1981_10