Hydrazine hydrate (1:1) → HCID 178505414, 화합물

HRID 717194

반응식

HRID 717194 반응식
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([NH2:8])=O)=[C:4]([F:11])[CH:3]=1.COC(OC)[N:15]([CH3:17])C.O.[NH2:21]N>C(O)(=O)C>[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]2[NH:15][CH:17]=[N:21][N:8]=2)=[C:4]([F:11])[CH:3]=1

참가 물질

5

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온도
85 °C

실험 절차

4-Bromo-2-fluorobenzamide (9.53 g, 43.7 mmol) and N,N-dimethylformamide dimethylacetal (75.0 mL) were combined in a 500 mL round bottom flask and purged with nitrogen. The reaction was heated to reflux at 85° C. for 2 h. The resulting mixture was concentrated under reduced pressure and dried under vacuum to afford a yellow oil. The oil was suspended in concentrated acetic acid (75.0 mL) and cooled to 0° C. Hydrazine hydrate (21.88 g, 437 mmol) was added dropwise and the mixture was allowed to stir at rt for 5 h. The reaction was poured warm onto cold ice and extracted with dichloromethane (3×200 mL). Organic volatiles were removed under reduced pressure to afford 3-(4-bromo-2-fluorophenyl)-4H-1,2,4-triazole (7.20 g, 29.7 mmol, 68.1% yield) as a white solid. MS (ESI) m/z 241.9 [M]+, 243.9 [M+2]+.

후처리

  1. custompurged with nitrogen
  2. temperatureThe reaction was heated
  3. concentrationThe resulting mixture was concentrated under reduced pressure
  4. customdried under vacuum
  5. customto afford a yellow oil
  6. temperaturecooled to 0° C
  7. additionThe reaction was poured
  8. temperaturewarm onto cold ice
  9. extractionextracted with dichloromethane (3×200 mL)
  10. customOrganic volatiles were removed under reduced pressure

출처 및 근거

ORD 기록
ord-fda8fa588132452f8a3977c5c7be6d01
출처 데이터셋
uspto-grants-2015_11
특허 번호
US09193692B2

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