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Acetic Acid → 2-carbamoyl-11-(3-dimethylaminopropylidene)-11H-pyrrolo[2,1-b][3]benzazepine

HRID 1763662
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반응식

HRID 1763662 반응식
[C:1]([C:3]1[CH:4]=[C:5]2[N:11]([CH:12]=1)[CH:10]=[CH:9][C:8]1[CH:13]=[CH:14][CH:15]=[CH:16][C:7]=1[C:6]2=[CH:17][CH2:18][CH2:19][N:20]([CH3:22])[CH3:21])#[N:2].Cl.C(O)(=[O:26])C>>[C:1]([C:3]1[CH:4]=[C:5]2[N:11]([CH:12]=1)[CH:10]=[CH:9][C:8]1[CH:13]=[CH:14][CH:15]=[CH:16][C:7]=1[C:6]2=[CH:17][CH2:18][CH2:19][N:20]([CH3:22])[CH3:21])(=[O:26])[NH2:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 176Acetic AcidHCID 313Hydrochloric AcidHCID 53685151HCID 53685151, 화합물

생성물 1

HCID 706269012-carbamoyl-11-(3-dimethylaminopropylidene)-11H-pyrrolo[2,1-b][3]benzazepine

실험 절차

2-Cyano-11-(3-dimethylaminopropylidene)-11H-pyrrolo[2,1-b][3]benzazepine (0.135 mole) in 100 ml. of concentrated hydrochloric acid and 100 ml. of acetic acid is refluxed for 2 hours. It is then poured onto 500 ml. of water and continuously extracted with methylene chloride. The solution is left to cool to room temperature and filtered to afford 2-carbamoyl-11-(3-dimethylaminopropylidene)-11H-pyrrolo[2,1-b][3]benzazepine.

후처리

  1. additionIt is then poured onto 500 ml
  • extractionof water and continuously extracted with methylene chloride
  • waitThe solution is left
  • filtrationfiltered
  • 출처 및 근거

    ORD 기록
    ord-10568e8f8e7b444b80812d79832b989b
    출처 데이터셋
    uspto-grants-1978_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04112112

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