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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 529427생성일: 2026년 10월 26일

Methanesulfonic Acid → HCID 178465174, 화합물

https://huagongshe.com/reaction/529427

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물L-Leucine, N-((1,1-dimethylethoxy)carbonyl)-HCID 83170—
반응물tert-Butoxycarbonyl-D-leucineHCID 637604—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물HCID 178465175HCID 178465175—
반응물HCID 178465176HCID 178465176—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물HCID 178465174HCID 178465174—

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346850B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-51863082633841f4bba1a33a8bd75953
출처 메모uspto-grants-2016_05