Dichloromethane → HCID 22418011、化合物

HRID 1728582ノート

反応式

HRID 1728582 の反応式
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

参加物

5

反応物 3

HCID 6344Dichloromethane2 回HCID 25134Boron tribromideHCID 19014342HCID 19014342、化合物

生成物 1

HCID 22418011HCID 22418011、化合物収率 75.5%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-767f16aba7a44a3f807228a6eb12259d
出典データセット
uspto-grants-1994_07
特許番号
US05328911

反応ノート

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