Methyl Anthranilate → Methyl 2-(3-chloro-4-methoxybenzamido)benzoate

HRID 2099969

反応式

HRID 2099969 の反応式
[NH2:1][C:2]1[CH:11]=[CH:10][CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].[Cl:12][C:13]1[CH:14]=[C:15]([CH:19]=[CH:20][C:21]=1[O:22][CH3:23])[C:16](O)=[O:17].CCN=C=NCCCN(C)C>CN(C=O)C.CN(C1C=CN=CC=1)C>[Cl:12][C:13]1[CH:14]=[C:15]([CH:19]=[CH:20][C:21]=1[O:22][CH3:23])[C:16]([NH:1][C:2]1[CH:11]=[CH:10][CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5])=[O:17]

参加物

6

反応物 3

HCID 8635Methyl AnthranilateHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 1699823-Chloro-p-anisic acid

生成物 1

HCID 800035Methyl 2-(3-chloro-4-methoxybenzamido)benzoate収率 33.2%

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒HCID 6228Dimethylformamide溶媒

実験手順

A solution of methyl 2-aminobenzoate (500 mg, 3.3 mmol) (Aldrich Chemical Co., Milwaukee, Wis.) and 3-chloro-4-methoxybenzoic acid (645 mg, 3.3 mmol) (Lancaster Synthesis Ltd., Windham, N.H.) in DMF (20 mL) was treated with EDCI (1.3 g, 6.6 mmol) and DMAP (800 mg, 6.6 mmol) at room temperature. The reaction mixture was stirred for 24 hours, and then concentrated. The crude residue was dissolved in EtOAc (50 mL) and washed with 0.1 N HCl (2×20 mL), saturated aqueous NaHCO3 (2×20 mL). The organic layer was dried (Na2SO4), filtered, and concentrated. The crude product was purified by chromatography (SiO2, 15% EtOAc in hexanes) to afford 42A as a white solid (350 mg, 33%).

後処理

  1. concentrationconcentrated
  2. dissolutionThe crude residue was dissolved in EtOAc (50 mL)
  3. washwashed with 0.1 N HCl (2×20 mL), saturated aqueous NaHCO3 (2×20 mL)
  4. dry with materialThe organic layer was dried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude product was purified by chromatography (SiO2, 15% EtOAc in hexanes)

出典と根拠

ORDレコード
ord-2ebb2b1e16f546d5ae3a5bb1b7b7de45
出典データセット
uspto-grants-2009_08
特許番号
US07569725B2

関連ノート

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