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Water → Quinoline-8-carboxamide

HRID 236870
ノート
印刷プレビュー

反応式

HRID 236870 の反応式
Cl[C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([C:12]([OH:14])=O)[CH:11]=1)[N:8]=[CH:7][CH:6]=[CH:5]2.C([N:17](CC)CC)C.COC(Cl)=O.O>CC(C)=O.CC1C=CC(CCN)=CC=1>[N:8]1[C:9]2[C:4](=[CH:3][CH:2]=[CH:11][C:10]=2[C:12]([NH2:17])=[O:14])[CH:5]=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 962WaterHCID 6586Methyl chloroformateHCID 8471TriethylamineHCID 1654926-Chloro-8-quinolinecarboxylic acid

生成物 1

HCID 150664Quinoline-8-carboxamide

試薬・触媒・溶媒 2

HCID 180Acetone溶媒2 回
HCID 76751
p-Methylphenethylamine
溶媒
2 回

実験手順

5.2 g of 6-chloro-quinoline-8-carboxylic acid in 150 ml of acetone were combined, while stirring and cooling with ice, with 2.8 g of triethylamine and 2.6 g of chloroformic acid methyl ester. The whole was stirred for about 10 minutes, a solution of 3.4 g of 2-(4-methylphenyl)-ethylamine in 50 ml of 2-(4-methylphenyl)-ethyl-amine in 50 ml of acetone was added and the mixture was again stirred for 1 hour at room temperature. Then, water was added, the precipitate was filtered off with suction, treated with a dilute ammonia solution, undissolved matter was filtered off and recrystallized from dilute methanol. The 6-chloro-N-(2-<4-methylphenyl>-ethyl)-quinoline-8-carboxylic acid amide so obtained was found to melt at 102°-104° C.

後処理

  1. stirringThe whole was stirred for about 10 minutes
  2. stirringthe mixture was again stirred for 1 hour at room temperature
  3. filtrationthe precipitate was filtered off with suction
  4. additiontreated with a dilute ammonia solution, undissolved matter
  5. filtrationwas filtered off
  6. customrecrystallized from dilute methanol

出典と根拠

ORDレコード
ord-b805e0eef3bd43c6aed0b139ab058722
出典データセット
uspto-grants-1979_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04158063

反応ノート

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