Triethylamine → HCID 67413214、化合物
反応式
[F:1][C:2]1[CH:24]=[C:23]([F:25])[CH:22]=[CH:21][C:3]=1[O:4][C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][C:13]=1[C:14](O)=[O:15])[N:10]([CH2:17][CH:18]([CH3:20])[CH3:19])[N:9]=[CH:8]2.C1C=CC2N(O)N=[N:32]C=2C=1.CCN=C=NCCCN(C)C.Cl.[CH3:48][O:49][C:50]1[CH:74]=[CH:73][C:53]([CH2:54][N:55]([CH:70]([CH3:72])[CH3:71])[CH2:56][CH2:57][C@H:58]([C:63]([O:65][C:66](C)(C)C)=[O:64])C(OC)=O)=[CH:52][CH:51]=1.C(N(CC)CC)C>ClC(Cl)C.ClCCl>[CH3:48][O:49][C:50]1[CH:51]=[CH:52][C:53]([CH2:54][N:55]([CH:70]([CH3:71])[CH3:72])[CH2:56][CH2:57][C@H:58]([NH:32][C:14]([C:13]2[CH:12]=[C:11]3[C:7]([CH:8]=[N:9][N:10]3[CH2:17][CH:18]([CH3:20])[CH3:19])=[CH:6][C:5]=2[O:4][C:3]2[CH:21]=[CH:22][C:23]([F:25])=[CH:24][C:2]=2[F:1])=[O:15])[C:63]([O:65][CH3:66])=[O:64])=[CH:73][CH:74]=1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
5-(2,4-Difluorophenoxy)-1-isobutyl-1H-indazole-6-carboxylic acid (17d; prepared according to Example 110) (0.022 g, 0.064 mmol) was stirred with HOBt (0.011 g, 0.070 mmol) and EDCI (0.014 g, 0.070 mmol) in dichloroethane (1 mL) for 10 minutes at room temperature. To this mixture was then added a suspension of (S)-methyl 4-((4-methoxybenzyl)(isopropyl)amino)-2-(tert-butoxycarbonyl)butanoate hydrochloride (0.025 g, 0.067 mmol) and triethylamine (0.054 mL, 0.384 mmol) in dichloromethane (2 mL). The mixture was stirred at room temperature for 16 hours. The solution was filtered through Celite and concentrated under reduced pressure. The crude oil was chromatographed eluting with 2% MeOH in dichloromethane with 1% triethylamine to provide 0.035 g of viscous pale yellow oil (89% yield).
後処理
- additionTo this mixture was then added
- filtrationThe solution was filtered through Celite
- concentrationconcentrated under reduced pressure
- customThe crude oil was chromatographed
- washeluting with 2% MeOH in dichloromethane with 1% triethylamine
出典と根拠
- ORDレコード
- ord-ca32863e00374364bcb0445515a67393
- 出典データセット
- uspto-grants-2013_08
- 特許番号
- US08518983B2
反応ノート
読み込み中…