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HRID 25571作成日:2026年10月24日

Sodium Iodide → HCID 178483981、化合物

https://huagongshe.com/ja/reaction/25571

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Sodium hydrideHCID 24758—
反応物Captamine HydrochlorideHCID 25798—
反応物Potassium bisulfateHCID 516920—
反応物Ether sodium bicarbonateHCID 23682952—
反応物HCID 178484820HCID 178484820—
溶媒DimethylformamideHCID 6228—
生成物HCID 178483981HCID 17848398163%

反応手順

A solution of 280 mg (0.5 mmol) of trans-4-Trifluoromethyl-benzenesulfonic acid 4-[methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexylmethyl ester and 78 mg (0.55 mmol) of 2-dimethylaminoethanethiol hydrochloride in 4.5 ml DMF was treated at 0° C. with 48 mg (1.1 mmol) of 55% NaH, stirred for 20 h at RT. After cooling (0° C.) and treatment with a catalytic amount of NaI followed by 78 mg (0.55 mmol) of 2-dimethylaminoethanethiol hydrochloride and 48 mg (1.1 mmol) of 55% NaH the reaction mixture was stirred for 18 h at RT. The reaction was neutralized (aqueous 10% KHSO4, at 0° C.) and poured into aqueous sat. NaHCO3/Et2O (3×). The organic phases were washed with aqueous 10% NaCl solution, dried over Na2SO4 and evaporated. Purification by flash column chromatography on silica gel with CH2Cl2/MeOH (95:5) yielded 138 mg (63%) of trans-N-[4-(2-Dimethylamino-ethylsulfanylmethyl)-cyclohexyl]-N-methyl-4-trifluoromethyl-benzenesulfonamide, MS: 439 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858651B2
出典データセットuspto-grants-2005_02
ORD IDord-b359497fad8842908e41ec30d66d9a0f
出典メモuspto-grants-2005_02