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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 727264생성일: 2026년 10월 24일

Water → (S)-N-(4-aminophenyl)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4, 3-a][1,4]diazepine-6-acetamide

https://huagongshe.com/ko/reaction/727264

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물P-PhenylenediamineHCID 7814—
반응물TriethylamineHCID 8471—
반응물2-((9S)-7-(4-chlorophenyl)-4,5,13-trimethyl-3-thia-1,8,11,12-tetraazatricyclo(8.3.0.0,2,6)trideca-2(6),4,7,10,12-pentaen-9-yl)acetic acidHCID 66828107—
용매DimethylformamideHCID 6228—
생성물(S)-N-(4-aminophenyl)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4, 3-a][1,4]diazepine-6-acetamideHCID 6897216415.2%

반응 단계

(S)-4-(4-Chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f]-[1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid (3.0 g), triethylamine (1.56 ml) and p-phenylenediamine (0.97 g) are dissolved in dimethylformamide (30 ml). Benzotriazol-1-yl-oxy-tris(dimethyl)phosphonium hexafluorophosphate (3.6 g) is added, and the mixture is stirred at room temperature for 12 hours. After the completion of the reaction, water (200 ml) is added, and the mixture is extracted with ethyl acetate. The extract is washed with saturated brine and dried over anhydrous magnesium sulfate. After the solvent is distilled away under reduced pressure, the residue is subjected to silica gel column chromatography and obtained crystals are recrystallized from toluene to give 0.56 g of (S)-N-(4-aminophenyl)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4, 3-a][1,4]diazepine-6-acetamide, melting point 169°-173° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05712274
출처 데이터셋uspto-grants-1998_01
ORD IDord-ead28fc17d244738af9fd38d986aa4a3
출처 메모uspto-grants-1998_01