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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 355897생성일: 2026년 10월 24일

Dibenzothiazepinone → N-[4-(11H-Dibenzo[b,f][1,4]thiazepine-10-carbonyl)-phenyl]-2-methyl-benzamide

https://huagongshe.com/ko/reaction/355897

반응식

참여 물질

역할이름HCID투입량
반응물DibenzothiazepinoneHCID 374829—
반응물4-[(2-methylbenzoyl)amino]benzoyl ChlorideHCID 10707441—
반응물10,11-Dihydrodibenzo(b,f)(1,4)thiazepineHCID 12310482—
반응물(Dimethyl sulfide)trihydroboronHCID 12423031—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
생성물N-[4-(11H-Dibenzo[b,f][1,4]thiazepine-10-carbonyl)-phenyl]-2-methyl-benzamideHCID 1530798816.9%

반응 단계

As described for in Reference Example 12, a mixture of 3.3 g of 10,11-dihydro-11-oxodibenz[b,f] [1,4]thiazepine, 25 ml of tetrahydrofuran, 4.0 ml of 10 molar borane-dimethylsulfide (2.67 equiyalents) in tetrahydrofuran is stirred at room temperature 18 hours to give, after work-up, 10,11-dihydrodibenz[b,f][1,4] thiazepine as white crystals, m.p. 145°-148° C. The preceding compound (3.5 g) is suspended in 25 ml of dichloromethane and a solution of 1.8 g of 4-[(2-methylbenzoyl) amino]benzoyl chloride in 50 ml of di-chloromethane added. To the stirred mixture is added 4 ml of triethylamine and 0.2 g of 4-(dimethylamino) pyridine. The mixture is stirred at room temperature for 20 hours. The mixture is filtered and the filtrate concentrated. The residue is purified by chromatography on silica gel with hexane-chloroform-ethyl acetate (2:1:1) as solyent to give 2.2 g of yel]ow crystals. A sample (0.80 g) is further purified by thick layer chromatography on silica gel with hexane-chloroform-ethyl acetate (2:1:1) as solvent to give 0.50 g of crystals, 76°-78° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05834461
출처 데이터셋uspto-grants-1998_11
ORD IDord-d939e207521c4d19bd111c843bed728f
출처 메모uspto-grants-1998_11