Tetrahydrofuran → 4,5-Diamino-3-chloro-2-phenylamino-benzoic acid methyl ester

HRID 217071

反応式

HRID 217071 の反応式
[CH3:1][O:2][C:3](=[O:22])[C:4]1[CH:9]=[C:8]([N+:10]([O-])=O)[C:7]([NH2:13])=[C:6]([Cl:14])[C:5]=1[NH:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.CCO.CO.[NH4+].[Cl-].C1COCC1>C(Cl)Cl.C1COCC1.O.[Zn]>[CH3:1][O:2][C:3](=[O:22])[C:4]1[CH:9]=[C:8]([NH2:10])[C:7]([NH2:13])=[C:6]([Cl:14])[C:5]=1[NH:15][C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1

参加物

8

反応物 4

HCID 8028TetrahydrofuranHCID 25517Ammonium ChlorideHCID 18681192Ethanol, mixt. with methanolHCID 858681964-Amino-3-chloro-5-nitro-2-phenylamino-benzoic acid methyl ester

生成物 1

HCID 858681984,5-Diamino-3-chloro-2-phenylamino-benzoic acid methyl ester収率 70.8%

試薬・触媒・溶媒 3

HCID 23994Zinc触媒HCID 962Water溶媒HCID 21919333Tetrahydrofurane dichloromethane溶媒

実験手順

4-Amino-3-chloro-5-nitro-2-phenylamino-benzoic acid methyl ester 5c (0.50 g, 1.55 mmol) is dissolved into 2:1 EtOH/MeOH (15.5 mL). Saturated aqueous NH4Cl (15 mL), Zn powder (1.02 g, 15.6 mmol), and THF (10 mL) are added. After stirring for 20 hours, the reaction mixture is diluted with CH2Cl2/THF and water. The organic layer is washed with water (3×). The combined organic extracts are dried (Na2SO4) and concentrated under reduced pressure. The solids are triturated with ether to give 0.32 g (70%) clean desired product.

後処理

  1. washThe organic layer is washed with water (3×)
  2. dry with materialThe combined organic extracts are dried (Na2SO4)
  3. concentrationconcentrated under reduced pressure
  4. customThe solids are triturated with ether

出典と根拠

ORDレコード
ord-5578053e37d0426f97e5645bfe047a76
出典データセット
uspto-grants-2012_06
特許番号
US08193231B2

関連ノート

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