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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25571생성일: 2026년 10월 24일

Sodium Iodide → HCID 178483981, 화합물

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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Sodium hydrideHCID 24758—
반응물Captamine HydrochlorideHCID 25798—
반응물Potassium bisulfateHCID 516920—
반응물Ether sodium bicarbonateHCID 23682952—
반응물HCID 178484820HCID 178484820—
용매DimethylformamideHCID 6228—
생성물HCID 178483981HCID 17848398163%

반응 단계

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+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858651B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-b359497fad8842908e41ec30d66d9a0f
출처 메모uspto-grants-2005_02