戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 260221作成日:2026年10月27日

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

https://huagongshe.com/reaction/260221

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物5,5'-Dithiobis(2-nitrobenzoic Acid)HCID 6254—
反応物Potassium HydroxideHCID 14797—
反応物3-Mercapto-N-methylpropanamideHCID 642906—
反応物(2-Carboxyphenyl)-sulfanylidene-sulfidoazaniumHCID 21865436—
反応物N-methyl-(3-thioacetyl)propionamideHCID 54417257—
反応物SMCC caproateHCID 131719433—
溶媒MethanolHCID 887—
溶媒Potassium Phosphate, TribasicHCID 62657—
生成物N-[4-(5-carboxypentylcarbamoyl)-cyclohexylmethyl]-2-(methylcarbamoyl)-ethylthiosuccinimideHCID 88051188—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05525524
出典データセットuspto-grants-1996_06
ORD IDord-84a161067fa441ecbd903aa4c6b6a1a5
出典メモuspto-grants-1996_06