Boron tribromide → HCID 57717495、化合物

HRID 1360577ノート

反応式

HRID 1360577 の反応式
B(Br)(Br)Br.[NH2:5][C:6]1[C:15]2=[N:16][N:17]([CH2:24][CH2:25][O:26]C)[C:18]([CH2:19][C:20]([CH3:23])([OH:22])[CH3:21])=[C:14]2[C:13]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[N:7]=1>ClCCl>[NH2:5][C:6]1[C:15]2=[N:16][N:17]([CH2:24][CH2:25][OH:26])[C:18]([CH2:19][C:20]([CH3:23])([OH:22])[CH3:21])=[C:14]2[C:13]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[N:7]=1

参加物

4

反応物 2

HCID 25134Boron tribromideHCID 57717561HCID 57717561、化合物

生成物 1

HCID 57717495HCID 57717495、化合物収率 24.1%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

Under a nitrogen atmosphere, boron tribromide (6 mL of a 1 M solution in dichloromethane) was added to a solution of 1-[4-amino-2-(2-methoxyethyl)-2H-pyrazolo[3,4-c]quinolin-1-yl]-2-methylpropan-2-ol (0.500 g, 1.59 mmol) in dichloromethane (8 mL), and the reaction was stirred for four hours. The dichloromethane was removed under reduced pressure, and the residue was dissolved in a mixture of ethanol and 3 N hydrochloric acid. A solution of 7 N ammonia in methanol was added, and then the solvent was removed under reduced pressure. The treatment with ammonia and the concentration were repeated two more times. The crude product was purified by chromatography using a HORIZON HPFC system (40+M cartridge, eluting with 0-30% CMA in chloroform) followed by trituration with acetonitrile and recrystallization from acetonitrile to provide 115 mg of 1-[4-amino-2-(2-hydroxyethyl)-2H-pyrazolo[3,4-c]quinolin-1-yl]-2-methylpropan-2-ol as white crystals, mp 196-198° C.

後処理

  1. customThe dichloromethane was removed under reduced pressure
  2. dissolutionthe residue was dissolved in a mixture of ethanol and 3 N hydrochloric acid
  3. additionA solution of 7 N ammonia in methanol was added
  4. customthe solvent was removed under reduced pressure
  5. concentrationThe treatment with ammonia and the concentration
  6. customThe crude product was purified by chromatography
  7. washa HORIZON HPFC system (40+M cartridge, eluting with 0-30% CMA in chloroform)
  8. customfollowed by trituration with acetonitrile and recrystallization from acetonitrile

出典と根拠

ORDレコード
ord-52799dbeaa72492599aa74406945b5b6
出典データセット
uspto-grants-2011_02
特許番号
US07879849B2

反応ノート

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