Dichloromethane → HCID 22418011, 화합물

HRID 1728582노트

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HRID 1728582 반응식
ClCCl.B(Br)(Br)Br.[CH3:8][O:9][C:10]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[C:18]1[CH:23]=[CH:22][C:21]([CH2:24][N:25]2[C:29]3=[N:30][CH:31]=[CH:32][C:33]([CH3:34])=[C:28]3[N:27]=[C:26]2[CH2:35][O:36]C)=[CH:20][CH:19]=1)=[O:11]>CO>[OH:36][CH2:35][C:26]1[N:25]([CH2:24][C:21]2[CH:22]=[CH:23][C:18]([C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=3[C:10]([O:9][CH3:8])=[O:11])=[CH:19][CH:20]=2)[C:29]2=[N:30][CH:31]=[CH:32][C:33]([CH3:34])=[C:28]2[N:27]=1

참가 물질

5

실험 절차

50 ml (50 retool) of a dichloromethane solution of 1M boron tribromide was added little by little dropwise to 100 ml of a dichloromethane solution of 3.3 g (8.2 mmol) of 3-[(2'-methoxycarbonyl-biphenyl-4-yl)methyl]-2-methoxymethyl-7-methyl-3H-imidazo[4.5-b]pyridine, while stirred and cooled with ice. The mixture was further stirred at a room temperature for 12 hours. Methanol was added dropwise to the product mixture, while stirred and cooled with ice, and the solvent was distilled out at a reduced pressure. The residue was mixed with water and neutralized with sodium bicarbonate. It was weakly acidified with acetic acid and decanted to remove the water. Methanol was added to the residue and distilled out at a reduced pressure. It was re-crystallized from ethanol-isopropylether to obtain 2.4 g of the intended compound.

후처리

  1. temperaturecooled with ice
  2. stirringThe mixture was further stirred at a room temperature for 12 hours
  3. stirringwhile stirred
  4. temperaturecooled with ice
  5. distillationthe solvent was distilled out at a reduced pressure
  6. additionThe residue was mixed with water and neutralized with sodium bicarbonate
  7. customdecanted
  8. customto remove the water
  9. additionMethanol was added to the residue
  10. distillationdistilled out at a reduced pressure
  11. customIt was re-crystallized from ethanol-isopropylether

출처 및 근거

ORD 기록
ord-767f16aba7a44a3f807228a6eb12259d
출처 데이터셋
uspto-grants-1994_07
특허 번호
US05328911

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