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HRID 258764作成日:2026年10月26日

Benzyloxycarbonylglycine → Benzyloxycarbonylaminoacetyl chloride

https://huagongshe.com/reaction/258764

反応式

関与物質

役割名称HCID仕込み量
反応物BenzyloxycarbonylglycineHCID 14349—
反応物Phosphorus pentachlorideHCID 24819—
溶媒Diethyl EtherHCID 3283—
生成物Benzyloxycarbonylaminoacetyl chlorideHCID 1223975976.6%

反応手順

A stirred mixture of N-benzyloxycarbonylglycine [30 g.; prepared as described in Ber., 65, 1192, (1932)] and dry diethyl ether (190 ml.) was treated at 0° C. with phosphorus pentachloride (32 g.) during 5 minutes. The mixture was stirred at between 0° and 5° C. for a further 20 minutes and the solution was then filtered and the filtrate was evaporated. The residue was triturated with petrol (b.p. 40°-60° C.) and the petrol layer was decanted off, and this procedure was repeated several times, keeping the temperature below 20° C. throughout. A solid formed, which was filtered off to give N-benzyloxycarbonylglycyl chloride (25 g.), which was used immediately in the next stage. N-Benzyloxycarbonylglycyl chloride (13.0 g.) was added in one portion to a stirred solution of 4-amino-3-(3-methoxycarbonyl-2-thioureido)diphenyl thioether (10.0 g.; prepared as hereinbefore described in Example 2) in dry dimethylformamide. The temperature of the mixture rose to 35° C., and the stirring was continued for 20 minutes. The solution was then poured into water. The resulting oil solidified on scratching. The solid was filtered off and recrystallised from a mixture of dimethylformamide and methanol to give 4-(2-benzyloxycarbonylaminoacetamido)-3-(3-methoxycarbonyl-2-thioureido)diphenyl thioether (13.0 g.), m.p. 184°-186° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04034107
出典データセットuspto-grants-1977_07
ORD IDord-7de60ff1800a4e83b8420e88af8b3be9
出典メモuspto-grants-1977_07