Hydrazine → HCID 178432644, 화합물

HRID 1401213노트

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HRID 1401213 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:9]([NH2:11])=O)=[N:6][C:7]=1[CH3:8].COC(OC)[N:15]([CH3:17])C.[NH2:20]N>C(O)(=O)C>[Br:1][C:2]1[C:7]([CH3:8])=[N:6][C:5]([C:9]2[N:11]=[CH:17][NH:15][N:20]=2)=[CH:4][CH:3]=1

참가 물질

5

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온도
85 °C

실험 절차

5-Bromo-6-methylpicolinamide (1 g, 4.65 mmol) and N,N-dimethylformamide dimethylacetal (20 mL) were combined in a 100 mL round-bottom flask with a stir bar and heated at 85° C. under a reflux condenser under nitrogen for 3 h. The resulting mixture was concentrated under reduced pressure and dried under vacuum to give yellow oil, which was used in the next step without purification. The residue was diluted with acetic acid (10 mL) and hydrazine (2.5 mL, 70.3 mmol) was added drop-wise and allowed to stir at room temperature for 5 h. The reaction mixture was poured into ice water. The resulting solid was filtered, washed with water and dried to give the desired product as a white solid. The aqueous filtrate was extracted with dichloromethane. The organic layer was concentrated under reduced pressure nearly to dryness to yield additional material. Combination of two batches gave the desired product (0.7 g, 2.9 mmol, 63% yield). MS (ESI) m/z 241.1 [M+2]+.

후처리

  1. concentrationThe resulting mixture was concentrated under reduced pressure
  2. customdried under vacuum
  3. customto give yellow oil, which
  4. customwas used in the next step without purification
  5. additionwas added drop-wise
  6. filtrationThe resulting solid was filtered
  7. washwashed with water
  8. customdried

출처 및 근거

ORD 기록
ord-b2c59b70a39e47c09a0e458e6fd8a4aa
출처 데이터셋
uspto-grants-2014_12
특허 번호
US08907087B2

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