反応式
C1(NC(C2C3C=C(C4C(C)=CN=C(NCCCC5CCCNC5)N=4)SC=3C=CC=2)=O)CC1.[CH:33]1([NH:36][C:37]([C:39]2[C:47]3[CH:46]=[C:45]([C:48]4[C:53]([Cl:54])=[CH:52][N:51]=[C:50](Cl)[N:49]=4)[S:44][C:43]=3[CH:42]=[CH:41][CH:40]=2)=[O:38])[CH2:35][CH2:34]1.C(OC([N:63]1[CH2:68][CH2:67][N:66]([CH2:69][CH2:70][CH2:71][NH2:72])[CH:65]([CH:73]([CH3:75])[CH3:74])[CH2:64]1)=O)(C)(C)C>>[CH:33]1([NH:36][C:37]([C:39]2[C:47]3[CH:46]=[C:45]([C:48]4[C:53]([Cl:54])=[CH:52][N:51]=[C:50]([NH:72][CH2:71][CH2:70][CH2:69][N:66]5[CH2:67][CH2:68][NH:63][CH2:64][CH:65]5[CH:73]([CH3:75])[CH3:74])[N:49]=4)[S:44][C:43]=3[CH:42]=[CH:41][CH:40]=2)=[O:38])[CH2:35][CH2:34]1参加物
4
反応物 3
生成物 1
実験手順
Using the method of racemic 2-[5-methyl-2-(3-piperidin-3-ylpropylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide, the title compound is synthesized from 2-(2,5-dichloropyrimidin-4-yl)-benzo[b]thiophene-4-carboxylic acid cyclopropylamide and racemic 4-(3-aminopropyl)-3-isopropylpiperazine-1-carboxylic acid tert-butyl ester and isolated as a solid. ES+(m/z) 513 (35Cl) and 515 (37Cl) [M+H].
後処理
- customisolated as a solid
出典と根拠
- ORDレコード
- ord-32196efdb52f43d0b29469559d0bf5e0
- 出典データセット
- uspto-grants-2009_06
- 特許番号
- US07547691B2
関連ノート
読み込み中…