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HRID 529427作成日:2026年10月26日

Methanesulfonic Acid → HCID 178465174、化合物

https://huagongshe.com/reaction/529427

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonic AcidHCID 6395—
反応物L-Leucine, N-((1,1-dimethylethoxy)carbonyl)-HCID 83170—
反応物tert-Butoxycarbonyl-D-leucineHCID 637604—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物HCID 178465175HCID 178465175—
反応物HCID 178465176HCID 178465176—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物HCID 178465174HCID 178465174—

反応手順

Boc-Leu-Arg(Ts)-Pro-NHEt was prepared from Boc-Arg(Ts)-Pro-NHEt obtained in Example 1 and Boc-Leu by the same procedure as Example 1. To a solution composed of the compound (0.969 g) and dichloromethane (10 ml), methanesulfonic acid (0.78 g) was added at room temperature, and the resulting mixture was stirred at room temperature for 4 hours, thereby the Boc group was removed (reaction conversion ratio: 100.0%). After the reaction, triethylamine in an amount of the same molar equivalent as that of the added methanesulfonic acid was added thereto, and the resulting mixture was stirred for 15 minutes. After Boc-D-Leu (0.40 g) and HOBt monohydrate (0.33 g) were added to the thus obtained dichloromethane solution of Leu-Arg(Ts)-Pro-NHEt, the reaction solution was cooled with ice. Then, EDC hydrochloride (0.42 g) was added thereto, and the resulting mixture was stirred for 1 hour. Subsequently, the temperature of the mixture was raised to room temperature and the mixture was stirred for 15 hours, thereby performing a condensation reaction (reaction conversion ratio: 100.0%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09346850B2
出典データセットuspto-grants-2016_05
ORD IDord-51863082633841f4bba1a33a8bd75953
出典メモuspto-grants-2016_05