Chloroacetamide → 3-Amino-7-carboxymethyl-4-thiophen-2-yl-6,7-dihydro-5H-cyclopenta[b]thieno[3,2-e]pyridine-2-carboxylic acid amide

HRID 2375366ノート

反応式

HRID 2375366 の反応式
[C:1]([C:3](=[CH:7][C:8]1[S:9][CH:10]=[CH:11][CH:12]=1)[C:4]([NH2:6])=[S:5])#[N:2].O=[C:14]1[CH2:18][CH2:17][CH2:16][CH:15]1[CH2:19][C:20]([OH:22])=[O:21].CN1CCOCC1.Cl[CH2:31][C:32]([NH2:34])=[O:33].C(=O)([O-])[O-].[K+].[K+]>C(O)C>[NH2:2][C:1]1[C:3]2[C:7]([C:8]3[S:9][CH:10]=[CH:11][CH:12]=3)=[C:18]3[CH2:17][CH2:16][CH:15]([CH2:19][C:20]([OH:22])=[O:21])[C:14]3=[N:6][C:4]=2[S:5][C:31]=1[C:32]([NH2:34])=[O:33]

参加物

7

実験手順

To a mixture of 2-cyano-3-thiophen-2-yl-thioacrylamide (6.3 g, 33 mmol), 2-oxocyclopentaneacetic acid (4.6 g, 33 mmol) in 70 ml of ethanol was added N-methylmorpholine (6.6 g, 65 mmol). The resulting mixture was refluxed overnight, then 2-chloroacetamide (6.1 g, 65 mmol) and anhydrous potassium carbonate (9.0 g, 65 mmol) was added with stirring. The reaction mixture was continued to reflux overnight. The reaction mixture was cooled to room temperature and the solid was filtered and washed with ethanol. The sodium salt of product was dissolved in 100 ml of water and neutralized with 10% hydrochloric acid to pH<6. The precipitate was filtered and washed with water to give 3.7 g (31%) of pure product as a yellow solid. 1H-NMR (300 MHz, DMSO-d6): δ 12.24 (brs, 1H), 7.87 (d, J=5.1 Hz, 1H), 7.27-7.24 (m, 2H), 7.18 (brs, 2H), 5.93 (brs, 2H), 3.55 (m, 1H), 2.94 (dd, J=3.9, 16.2 Hz, 1H), 2.68 (m, 2H), 2.40 (m, 2H), 1.75 (m, 1H). ES MS m/z 374 (M+H)+, 372 (M−H)−.

後処理

  1. temperatureThe resulting mixture was refluxed overnight
  2. temperatureto reflux overnight
  3. filtrationthe solid was filtered
  4. washwashed with ethanol
  5. dissolutionThe sodium salt of product was dissolved in 100 ml of water and neutralized with 10% hydrochloric acid to pH<6
  6. filtrationThe precipitate was filtered
  7. washwashed with water

出典と根拠

ORDレコード
ord-9d4775d427f8496ea98a351c0927bdbf
出典データセット
uspto-grants-2008_12
特許番号
US07465742B2

反応ノート

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