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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 260221생성일: 2026년 10월 26일

Hydrochloric Acid → N-[4-(5-carboxypentylcarbamoyl)-cyclohexylmethyl]-2-(methylcarbamoyl)-ethylthiosuccinimide

https://huagongshe.com/reaction/260221

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물5,5'-Dithiobis(2-nitrobenzoic Acid)HCID 6254—
반응물Potassium HydroxideHCID 14797—
반응물3-Mercapto-N-methylpropanamideHCID 642906—
반응물(2-Carboxyphenyl)-sulfanylidene-sulfidoazaniumHCID 21865436—
반응물N-methyl-(3-thioacetyl)propionamideHCID 54417257—
반응물SMCC caproateHCID 131719433—
용매MethanolHCID 887—
용매Potassium Phosphate, TribasicHCID 62657—
생성물N-[4-(5-carboxypentylcarbamoyl)-cyclohexylmethyl]-2-(methylcarbamoyl)-ethylthiosuccinimideHCID 88051188—

반응 단계

The thiol ester of N-methyl-(3-thioacetyl)-propionamide (4.6 mg, 3.1×10-5 mol, see Example 3) was hydrolyzed by the addition of 0.62 ml of 0.12M KOH in 80% methanol. After 10 min, 0.3 ml of 0.5M potassium phosphate, pH 7 was added to the thiol compound and the pH adjusted to 7.5 with 1N hydrochloric acid. The thiol concentration was 34 mM (determined by reaction with dithionitrobenzoic acid, DTNB). SMCC-caproate (8.7 mg, 2.5×10-5 mol) was dissolved in 0.4 ml of 0.5M potassium phosphate, pH 7.0, and the N-methyl-(3-mercapto)propionamide solution (0.742 ml, 2.5×10-5 mol) added. The solution was gassed with argon and the tube sealed. After 12 hr at room temperature, no thiol remained and the solvent was removed in vacuo. The residue was dissolved in 0.117 ml water to make a 213 mM solution of the desired compound (see FIG. 1D).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05525524
출처 데이터셋uspto-grants-1996_06
ORD IDord-84a161067fa441ecbd903aa4c6b6a1a5
출처 메모uspto-grants-1996_06