반응식
[Cl:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[NH2:8].[NH2:9][C:10]1[C:11]([C:25](O)=[O:26])=[N:12][C:13]([C:17]2[C:22]([F:23])=[CH:21][CH:20]=[CH:19][C:18]=2[F:24])=[C:14]([F:16])[CH:15]=1.C1C=NC2N(O)N=NC=2C=1.CCN=C=NCCCN(C)C>CN1C(=O)CCC1>[NH2:9][C:10]1[C:11]([C:25]([NH:8][C:3]2[CH:4]=[N:5][CH:6]=[CH:7][C:2]=2[Cl:1])=[O:26])=[N:12][C:13]([C:17]2[C:18]([F:24])=[CH:19][CH:20]=[CH:21][C:22]=2[F:23])=[C:14]([F:16])[CH:15]=1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a solution of 4-chloropyridin-3-amine (1.0 equiv.) and 3-amino-6-(2,6-difluorophenyl)-5-fluoropicolinic acid (1.0 equiv.) in NMP (1 M) was added HOAt and EDCI sequentially. The reaction mixture was stirred at room temperature for 2 days. The crude reaction was purified by prep HPLC to give 3-amino-N-(4-chloropyridin-3-yl)-6-(2,6-difluorophenyl)-5-fluoropicolinamide (14%). LCMS (m/z): 379.0 (MH+); LC Rt=3.49 min
후처리
- customThe crude reaction
- customwas purified by prep HPLC
출처 및 근거
- ORD 기록
- ord-c2a9a24737da4afeb34ee92ab5fc4609
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08822497B2
연결된 노트
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