Methane → 2-methoxy-6-[(N-2-aminophenyl)-amino]-8-methylquinoline

HRID 1198939ノート

反応式

HRID 1198939 の反応式
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[C:6]([CH3:23])[CH:7]=[C:8]([NH:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[N+:20]([O-])=O)[CH:9]=2)[N:4]=1.C>C(O)C>[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[C:6]([CH3:23])[CH:7]=[C:8]([NH:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=3[NH2:20])[CH:9]=2)[N:4]=1

参加物

4

反応物 2

HCID 297MethaneHCID 198677162-methoxy-6[(N-2-nitrophenyl)-amino]-8-methylquinoline

生成物 1

HCID 544931382-methoxy-6-[(N-2-aminophenyl)-amino]-8-methylquinoline

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A solution of 2-methoxy-6[(N-2-nitrophenyl)-amino]-8-methylquinoline (0.2 g) in absolute ethanol (20 cm3) was hydrogenated at 60° and 60 p.s.i. (4.13×105Pa) pressure over 10% palladised charcoal (0.03 g) for 4 hours. The cooled solution was then filtered through "Solkafloc" (Trade Mark for a cellulose-based filtering aid), evaporated to dryness in vacuo, characterised spectroscopically and used directly in Preparation 16 without further purification.

後処理

  1. customwas hydrogenated at 60°
  2. filtrationThe cooled solution was then filtered through "Solkafloc" (Trade Mark for a cellulose-
  3. filtrationbased filtering aid),
  4. customevaporated to dryness in vacuo
  5. customused directly in Preparation 16 without further purification

出典と根拠

ORDレコード
ord-d0df142ccb79462fafa1647de8069b65
出典データセット
uspto-grants-1990_02
特許番号
US04898872

反応ノート

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