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
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
反応物 4
生成物 1
試薬・触媒・溶媒 1
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
- temperatureThe mixture is refluxed overnight
- customto return to ambient temperature
- customPurification
- washis carried out on a silica column, elution being
- customThe oil obtained
- 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
読み込み中…