Allylamine → N-allyl-2-chloro-3-nitroquinolin-4-amine

HRID 606032

反応式

HRID 606032 の反応式
C(N(CC)CC)C.[Cl:8][C:9]1[C:18]([N+:19]([O-:21])=[O:20])=[C:17](Cl)[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[N:10]=1.[CH2:23]([NH2:26])[CH:24]=[CH2:25]>ClCCl>[CH2:23]([NH:26][C:17]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[N:10]=[C:9]([Cl:8])[C:18]=1[N+:19]([O-:21])=[O:20])[CH:24]=[CH2:25]

参加物

5

反応物 3

HCID 7853AllylamineHCID 8471TriethylamineHCID 27851382,4-Dichloro-3-nitroquinoline

生成物 1

HCID 59007293N-allyl-2-chloro-3-nitroquinolin-4-amine収率 105.2%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

Triethylamine (17.0 mL, 123 mmol) was added to a 0° C. solution of 2,4-dichloro-3-nitroquinoline (20.0 g, 82.3 mmol) in dichloromethane (350 mL) followed by the dropwise addition of allylamine (5.90 mL, 78.2 mmol). The solution was allowed to stir and warm to room temperature overnight. The solvent was evaporated under reduced pressure and the resulting orange solid was suspended in water (300 mL). Solid sodium carbonate was added to adjust the pH to 10-11 and the suspension was stirred for 2 hours at 0° C. A yellow solid was isolated by filtration and dried under vacuum overnight to yield N-allyl-2-chloro-3-nitroquinolin-4-amine (21.7 g) that contained small amounts of an impurity and water.

後処理

  1. customThe solvent was evaporated under reduced pressure
  2. additionSolid sodium carbonate was added
  3. stirringthe suspension was stirred for 2 hours at 0° C
  4. customA yellow solid was isolated by filtration
  5. customdried under vacuum overnight

出典と根拠

ORDレコード
ord-7533faf04dc6419f89e9b1ab9f5be9e6
出典データセット
uspto-grants-2011_03
特許番号
US07915281B2

関連ノート

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