p-Toluenesulfonic acid → (4-amino-6-methyl-2,3-dihydro-1H-8-thia-7-aza-cyclopenta[a]inden-5-yl)-cyclopropyl-methanone

HRID 133543

反応式

HRID 133543 の反応式
[NH2:1][C:2]1[S:6][C:5]2[CH2:7][CH2:8][CH2:9][C:4]=2[C:3]=1[C:10]#[N:11].[CH:12]1([C:15](=[O:21])[CH:16]=[C:17](OC)[CH3:18])[CH2:14][CH2:13]1.C1(C)C=CC(S(O)(=O)=O)=CC=1.[Sn](Cl)(Cl)(Cl)Cl>C1(C)C=CC=CC=1>[NH2:11][C:10]1[C:3]2[C:4]3[CH2:9][CH2:8][CH2:7][C:5]=3[S:6][C:2]=2[N:1]=[C:17]([CH3:18])[C:16]=1[C:15]([CH:12]1[CH2:14][CH2:13]1)=[O:21]

参加物

6

実験手順

To a stirred solution of 0.30 g (1.83 mmol) of 2-amino-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carbonitrile in 6 ml toluene was added 0.30 g (2.14 mmol) 1-cyclopropyl-3-methoxy-but-2-en-1-one and 3 mg of p-toluenesulfonic acid. The mixture was heated at reflux for 2 hours, concentrated in vacuo, partitioned between ethyl acetate and water. The combined organic phases were dried over sodium sulfate and evaporated to dryness. The residue was taken up in n-butyl acetate 6 ml and 1.018 g (3.91 mmol) tin (IV) chloride was heated under reflux for 30 minute and allowed to cool. The mixture was partitioned between aqueous sodium hydroxide and ethyl acetate. Flash chromatography (heptane/ethyl acetate 3:1) afforded 25 mg (5%) (4-amino-6-methyl-2,3-dihydro-1H-8-thia-7-aza-cyclopenta[a]inden-5-yl)-cyclopropyl-methanone as a white solid. ES-MS m/e (%): 273 (M+H+, 100).

後処理

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 2 hours
  3. concentrationconcentrated in vacuo
  4. custompartitioned between ethyl acetate and water
  5. dry with materialThe combined organic phases were dried over sodium sulfate
  6. customevaporated to dryness
  7. temperatureunder reflux for 30 minute
  8. temperatureto cool
  9. customThe mixture was partitioned between aqueous sodium hydroxide and ethyl acetate

出典と根拠

ORDレコード
ord-9c25546f3df240cdb6cad1c6fefddfc2
出典データセット
uspto-grants-2008_06
特許番号
US07390903B2

関連ノート

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