Stannous chloride dihydrate → 4-Amino-2-(3,5-dimethylphenyl)benzoyl methionine methyl ester

HRID 1739144ノート

反応式

HRID 1739144 の反応式
[CH3:1][O:2][C:3](=[O:29])[C@H:4]([CH2:25][CH2:26][S:27][CH3:28])[NH:5][C:6](=[O:24])[C:7]1[CH:12]=[CH:11][C:10]([N+:13]([O-])=O)=[CH:9][C:8]=1[C:16]1[CH:21]=[C:20]([CH3:22])[CH:19]=[C:18]([CH3:23])[CH:17]=1.O.O.Cl[Sn]Cl.COC(=O)[C@H](CCSC)NC(=O)C1C=CC(N)=CC=1C1C=CC=CC=1>C(OCC)(=O)C>[CH3:1][O:2][C:3](=[O:29])[C@H:4]([CH2:25][CH2:26][S:27][CH3:28])[NH:5][C:6](=[O:24])[C:7]1[CH:12]=[CH:11][C:10]([NH2:13])=[CH:9][C:8]=1[C:16]1[CH:17]=[C:18]([CH3:23])[CH:19]=[C:20]([CH3:22])[CH:21]=1

参加物

5

実験手順

4-nitro-2-(3,5-dimethylphenyl)benzoyl methionine methyl ester (0.11 g, 0.26 mmol) was taken up in ethyl acetate (3.0 ml). To this mixture was added SnCl2.2H2O (0.30 g, 1.30 mmol) and the reaction was heated under nitrogen at reflux for 6 h. The mixture was worked up as described for 4-amino-2-phenylbenzoyl methionine methyl ester in Example 2, to give 0.15 g of a yellow film that was wet with solvent. The material was otherwise pure by NMR and was used without further purification. 1H NMR (CDCl3) 1.60-1.70 (1H, m), 1.80-1.90 (1H, m), 1.99 (3H, s), 2.05 (2H, t, J=7.6 Hz), 2.33 (6H, s), 3.64 (3H, s), 3.93 (2H, br s), 4.61-4.64 (1H, m), 5.82 (1H, d, J=7.7 Hz), 6.49 (1H, d, J=2.3 Hz), 6.62 (1H, dd, J=8.4 Hz, 2.4 Hz), 6.98 (2H, s), 7.00 (1H, s), 7.65 (1H, d, J=8.3 Hz); 13C NMR (CDCl3) 15.08, 21.17, 29.28, 31.49, 51.70, 52.18, 113.30, 115.94, 123.55, 126.36, 129.32, 131.23, 138.15, 140.72, 141.92, 148.40, 168.45, 172.01.

後処理

  1. temperaturethe reaction was heated under nitrogen
  2. temperatureat reflux for 6 h
  3. customto give 0.15 g of a yellow film that
  4. customwas used without further purification

出典と根拠

ORDレコード
ord-24d6d8f55a9043dcbf1d5c6d1347d300
出典データセット
uspto-grants-1999_10
特許番号
US05965539

反応ノート

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