Methanol → 4-(6-Fluoro-3,4-dihydroxyphenyl)-1,2,3,4-tetrahydroisoquinoline hydrobromide

HRID 54682

反応式

HRID 54682 の反応式
[F:1][C:2]1[C:7]([CH:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH2:11][NH:10][CH2:9]2)=[CH:6][C:5]([O:18]C)=[C:4]([O:20]C)[CH:3]=1.B(Br)(Br)[Br:23].ClCCl.CO>ClCCl.C(=O)=O.CO>[BrH:23].[F:1][C:2]1[C:7]([CH:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH2:11][NH:10][CH2:9]2)=[CH:6][C:5]([OH:18])=[C:4]([OH:20])[CH:3]=1

参加物

6

反応物 3

HCID 887MethanolHCID 19959712HCID 19959712、化合物HCID 22277759Boron tribromide dichloromethane

生成物 1

HCID 147195754-(6-Fluoro-3,4-dihydroxyphenyl)-1,2,3,4-tetrahydroisoquinoline hydrobromide

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 21973728Carbon dioxide methanol溶媒

実験手順

1.15 g of 4-(6-fluoro-3,4-dimethoxyphenyl)-1,2,3,4-tetrahydroisoquinoline was dissolved in 30 ml of dichloromethane, 26.4 ml of 1M boron tribromide-dichloromethane solution was added to the solution under an argon gas stream under stirring under cooling at the internal temperature of -20° to -30° C. The mixture was stirred for 3 hours at room temperature, and then, 7.0 ml of methanol was added dropwise under cooling in dry ice-methanol bath. The mixture was stirred for 30 minutes at room temperature, the crystals which separated out were collected by filtration, affording 1.0 g of 4-(6-fluoro-3,4-dihydroxyphenyl)-1,2,3,4-tetrahydroisoquinoline hydrobromide.

後処理

  1. temperatureunder cooling at the internal temperature of -20° to -30° C
  2. stirringThe mixture was stirred for 3 hours at room temperature
  3. stirringThe mixture was stirred for 30 minutes at room temperature
  4. customthe crystals which separated out
  5. filtrationwere collected by filtration

出典と根拠

ORDレコード
ord-f4f1410458e34e6ba1c85a448576615c
出典データセット
uspto-grants-1997_04
特許番号
US05623074

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