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Ammonia → 2-Naphthalenecarboxamide, 5,6-dihydro-7-(1H-imidazol-1-yl)-

HRID 1980548
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HRID 1980548 반응식
[N:1]1([C:6]2[CH2:7][CH2:8][C:9]3[C:14]([CH:15]=2)=[CH:13][C:12]([C:16]([OH:18])=O)=[CH:11][CH:10]=3)[CH:5]=[CH:4][N:3]=[CH:2]1.[NH3:19]>CN(C=O)C>[N:1]1([C:6]2[CH2:7][CH2:8][C:9]3[C:14]([CH:15]=2)=[CH:13][C:12]([C:16](=[O:18])[NH2:19])=[CH:11][CH:10]=3)[CH:5]=[CH:4][N:3]=[CH:2]1
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참가 물질

4

반응물 2

HCID 222AmmoniaHCID 56009Rolafagrel

생성물 1

HCID 30215672-Naphthalenecarboxamide, 5,6-dihydro-7-(1H-imidazol-1-yl)-

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a suspension of 1,2-dihydro-3-(1-imidazolyl)-6-carboxy-naphthalene (500 mg) in DMF (10 ml) SOCl2 (2 ml) was added. Cooling in an ice bath, NH3 was passed through the reaction mixture, with stirring, for 5 hours. The reaction mixture was allowed to stand for 12 hours. The ammonium salt was filtered off and Et2O was added giving a precipitate which was chromatographed on silica gel with CHCl3 :CH3OH:CH3COOH (45:5:2.5) as eluant; 350 mg of 1,2-dihydro-3-(1-imidazolyl)-6-carbamoyl-naphthalene were obtained.

후처리

  1. additionwas added
  2. temperatureCooling in an ice bath
  3. waitto stand for 12 hours
  4. filtrationThe ammonium salt was filtered off
  5. additionEt2O was added
  6. customgiving a precipitate which
  7. customwas chromatographed on silica gel with CHCl3 :CH3OH:CH3COOH (45:5:2.5) as eluant

출처 및 근거

ORD 기록
ord-ebb4d65296ac4506a6d20c993e91dadf
출처 데이터셋
uspto-grants-1985_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04510149

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