Methanol → 3-(2,4-Dichlorophenyl)-6-(2-ethyl-5-hydroxymethyl-2H-pyrazol-3-yl) 1,9-dimethyl-1,9-dihydropyrido[2,3-b]indol-2-one

HRID 559161ノート

反応式

HRID 559161 の反応式
C([O:3][C:4]([C:6]1[CH:10]=[C:9]([C:11]2[CH:12]=[C:13]3[C:17](=[CH:18][CH:19]=2)[N:16]([CH3:20])[C:15]2[N:21]([CH3:34])[C:22](=[O:33])[C:23]([C:25]4[CH:30]=[CH:29][C:28]([Cl:31])=[CH:27][C:26]=4[Cl:32])=[CH:24][C:14]3=2)[N:8]([CH2:35][CH3:36])[N:7]=1)=O)C.[BH4-].[Na+].C(Cl)Cl.CO>C(O)C>[Cl:32][C:26]1[CH:27]=[C:28]([Cl:31])[CH:29]=[CH:30][C:25]=1[C:23]1[C:22](=[O:33])[N:21]([CH3:34])[C:15]2[N:16]([CH3:20])[C:17]3[C:13]([C:14]=2[CH:24]=1)=[CH:12][C:11]([C:9]1[N:8]([CH2:35][CH3:36])[N:7]=[C:6]([CH2:4][OH:3])[CH:10]=1)=[CH:19][CH:18]=3

参加物

6

実験手順

450 mg (0.86 mmol) of compound from Example 59, 5-[3-(2,4-dichlorophenyl)-1,9-dimethyl-2-oxo-2,9-dihydro-1H-pyrido[2,3-b]indol-6-yl]-1-ethyl-1H-pyrazole-3-carboxylic acid ethyl ester, are dissolved in 10 ml of absolute ethanol and 42 mg (1.12 mmol) of NaBH4 are added. The mixture is refluxed overnight. The reaction medium is allowed to return to ambient temperature, CH2Cl2 and MeOH are added, and the product is adsorbed onto silica. Purification is carried out on a silica column, elution being carried our with EtOAc, and then with a 95/05 EtOAc/MeOH mixture. The oil obtained is triturated in ether.

後処理

  1. temperatureThe mixture is refluxed overnight
  2. customto return to ambient temperature
  3. customPurification
  4. washis carried out on a silica column, elution being
  5. customThe oil obtained
  6. customis triturated in ether

出典と根拠

ORDレコード
ord-e52744583549405594a5518c4cf643b1
出典データセット
uspto-grants-2011_11
特許番号
US08063061B2

反応ノート

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