反応式
Cl.CN(C)CCCN=C=NCC.C1C=CC2N(O)N=NC=2C=1.[CH:23]1([NH2:28])[CH2:27][CH2:26][CH2:25][CH2:24]1.[N:29]1[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=1[C:35]1[C:36]([C:43]2[C:52]3[C:47](=[CH:48][C:49]([C:53](O)=[O:54])=[CH:50][CH:51]=3)[N:46]=[CH:45][CH:44]=2)=[C:37]2[CH2:42][CH2:41][CH2:40][N:38]2[N:39]=1>ClCCl>[CH:23]1([NH:28][C:53]([C:49]2[CH:48]=[C:47]3[C:52]([C:43]([C:36]4[C:35]([C:30]5[CH:31]=[CH:32][CH:33]=[CH:34][N:29]=5)=[N:39][N:38]5[CH2:40][CH2:41][CH2:42][C:37]=45)=[CH:44][CH:45]=[N:46]3)=[CH:51][CH:50]=2)=[O:54])[CH2:27][CH2:26][CH2:25][CH2:24]1参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
A mixture of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, (53 mg, 0.30 mmol), HOBT, (24 mg, 0.28 mmol), cyclopentylamine (0.03 mL, 0.30 mmol), and 4-(2-pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-quinoline-7-carboxylic acid (90 mg, 0.25 mmol) in dichloromethane (1 mL) is stirred room temperature for 18 h. The mixture is concentrated in vacuo and the residue chromatographed on SiO2 to yield the title compound, 31 mg (31%,) as a white solid.
後処理
- concentrationThe mixture is concentrated in vacuo
- customthe residue chromatographed on SiO2
出典と根拠
- ORDレコード
- ord-7e43ca3ac0294abfb9cc8c732e641078
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07087626B2
関連ノート
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