Acetic Acid → 4-(3-chloro-phenylamino)-3-[3-(methylaminocarbonyl)-benzylamino]-1H-pyrazolo[3,4-d]pyrimidine
反応式
[NH2:1][C:2]1[C:10]2[C:5](=[N:6][CH:7]=[N:8][C:9]=2[NH:11][C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([Cl:18])[CH:13]=2)[NH:4][N:3]=1.[CH3:19][NH:20][C:21]([C:23]1[CH:24]=[C:25]([CH:28]=[CH:29][CH:30]=1)[CH:26]=O)=[O:22].C(O)(=O)C.[BH3-]C#N.[Na+]>CO.CN1C(=O)N(C)CC1>[Cl:18][C:14]1[CH:13]=[C:12]([NH:11][C:9]2[N:8]=[CH:7][N:6]=[C:5]3[NH:4][N:3]=[C:2]([NH:1][CH2:26][C:25]4[CH:28]=[CH:29][CH:30]=[C:23]([C:21]([NH:20][CH3:19])=[O:22])[CH:24]=4)[C:10]=23)[CH:17]=[CH:16][CH:15]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
A solution of 261 mg (1.0 mmol) of 3-amino-4-(3-chloro-phenylamino)-1H-pyrazolo[3,4-d]pyrimidine (see Step 15.1) and 245 mg (1.5 mmol) of 3-(methylamino-carbonyl)-benzaldehyde in 26 ml of methanol, 26 ml of DMEU and 180 mg (3.0 mmol) of acetic acid is stirred for 1 hour at RT. Then 440 mg (7.0 mmol) of NaCNBH3 are added and the reaction mixture is stirred for 9 days at RT. The methanol is evaporated off from the reaction solution using a rotary evaporator, the residue is poured into 0.6 liter of water and stirring is carried out overnight. The product precipitates. Filtering with suction, washing with water, stirring twice in 10 ml of boiling ethanol, cooling and filtering yield 4-(3-chloro-phenylamino)-3-[3-(methylaminocarbonyl)-benzylamino]-1H-pyrazolo[3,4-d]pyrimidine; m.p. 252-254° C.; HPLC: TRet (Grad5-40)=16.9; FAB-MS: (M+H)+ =408.
後処理
- customThe methanol is evaporated off from the reaction solution
- customa rotary evaporator
- additionthe residue is poured into 0.6 liter of water
- stirringstirring
- waitis carried out overnight
- customThe product precipitates
- filtrationFiltering with suction
- washwashing with water
- stirringstirring twice in 10 ml of boiling ethanol
- temperaturecooling
- filtrationfiltering
出典と根拠
- ORDレコード
- ord-42586daa614943f0850bdb2f30f7c12a
- 出典データセット
- uspto-grants-1999_11
- 特許番号
- US05981533
反応ノート
読み込み中…