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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1606041생성일: 2026년 10월 26일

Sodium Carbonate → 6-o-chlorophenyl-8-ethyl-4H-tetrazolo[5,1-c]thieno[2,3-e] [1,4]diazepine

https://huagongshe.com/reaction/1606041

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물2-hydrazino-5-o-chlorophenyl-7-ethyl-3H-thieno[2,3-e][1,4]diazepineHCID 12434299—
반응물Sodium NitriteHCID 23668193—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
생성물6-o-chlorophenyl-8-ethyl-4H-tetrazolo[5,1-c]thieno[2,3-e] [1,4]diazepineHCID 5453554979.3%

반응 단계

[f] 10 g of 2-hydrazino-5-o-chlorophenyl-7-ethyl-3H-thieno[2,3-e][1,4]diazepine prepared in the above example [d] is suspended in 54 ml of 2N hydrochloric acid. A solution of 2.4 g of sodium nitrite in 20 ml of water is added to the suspension at -5°C with stirring. The mixture is stirred at room temperature for 30 minutes, and then alkalified with sodium carbonate. The precipitated crystals are filtered off and dissolved in chloroform, and the solution is washed with water. The chloroform layer is dried over anhydrous magnesium sulfate, and the chloroform is distilled off under reduced pressure. The reddish brown jellylike residue thus obtained is crystallized from a mixture of ligroin and ethanol to give 8.2 g of 6-o-chlorophenyl-8-ethyl-4H-tetrazolo[5,1-c]thieno[2,3-e] [1,4]diazepine as white crystals. The product, when recrystallized from ethanol, melts at 135° - 136°C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03952006
출처 데이터셋uspto-grants-1976_04
ORD IDord-0e4c796d5c3441c3bd35cceb2000c360
출처 메모uspto-grants-1976_04