Isobutylamine → 4-Isobutyl-3-nitro quinoline

HRID 1375152

反応式

HRID 1375152 の反応式
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[N+:12]([O-:14])=[O:13].[CH2:15](N)[CH:16]([CH3:18])[CH3:17].N(CCO)(CCO)CCO>C1(C)C=CC=CC=1>[CH2:15]([C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[N+:12]([O-:14])=[O:13])[CH:16]([CH3:18])[CH3:17]

参加物

5

反応物 3

HCID 6558IsobutylamineHCID 7618TriethanolamineHCID 112758084-Chloro-3-nitroquinoline

生成物 1

HCID 225904984-Isobutyl-3-nitro quinoline

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

4-chloro-3-nitro-quinoline is reacted with isobutyl amine in the presence of triethanolamine (TEA) at between −10 and +15° C. in toluene, while excluding moisture. After washing and phase separation, the organic solution is ready for the next step.

後処理

  1. washAfter washing
  2. customphase separation

出典と根拠

ORDレコード
ord-141466dddea84eadb5617a749c199086
出典データセット
uspto-grants-2007_01
特許番号
US07166721B2

関連ノート

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