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Benzonitrile, 4-bromo- → 6-(4-bromophenyl)-5H-thieno[3,2-c]pyridin-4-one

HRID 1251172
ノート
印刷プレビュー

反応式

HRID 1251172 の反応式
[CH3:1][NH:2][C:3]([C:5]1[CH:9]=[CH:8][S:7][C:6]=1[CH3:10])=[O:4].C([Li])CCC.[Br:16][C:17]1[CH:24]=[CH:23][C:20](C#N)=[CH:19][CH:18]=1>O1CCCC1>[Br:16][C:17]1[CH:24]=[CH:23][C:20]([C:1]2[NH:2][C:3](=[O:4])[C:5]3[CH:9]=[CH:8][S:7][C:6]=3[CH:10]=2)=[CH:19][CH:18]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 12162Benzonitrile, 4-bromo-HCID 22503091n-Methyl-2-methylthiophene-3-carboxamideHCID 178418339Butyllithium

生成物 1

HCID 225024536-(4-bromophenyl)-5H-thieno[3,2-c]pyridin-4-one収率 19.1%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-70 °C

実験手順

To a solution of N-methyl-2-methylthiophene-3-carboxamide (13.0 g) in tetrahydrofuran (130 ml) was dropwise added 2.5 M butyl lithium (74 ml) at −70° C. The reaction solution was stirred at −70° C. for 2 hr, followed by the addition of 4-bromobenzonitrile (15.3 g) at once. After the dry ice/acetone bath was removed, the reaction mixture was back to room temperature. Three hours later, an aqueous solution of saturated ammonium chloride and ether were added thereto, and then the resulting mixture was further stirred for 1 hr. The resulting white precipitates were collected by filtration, and washed with water, ether and n-hexane in this order. The resulting product was dried to give the title compound (4.9 g, yield; 19%).

後処理

  1. customat −70° C
  2. customAfter the dry ice/acetone bath was removed
  3. customwas back to room temperature
  4. additionThree hours later, an aqueous solution of saturated ammonium chloride and ether were added
  5. stirringthe resulting mixture was further stirred for 1 hr
  6. customThe resulting white precipitates
  7. filtrationwere collected by filtration
  8. washwashed with water, ether and n-hexane in this order
  9. customThe resulting product was dried

出典と根拠

ORDレコード
ord-e902df5f1ba646289af58d7b28dc76ae
出典データセット
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06340759B1

反応ノート

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