Allitinib metabolite M6 → HCID 67335614, compound
Reaction equation
CO[C:3](=O)[CH2:4][CH2:5][C@H:6]([NH2:37])[C:7](=[O:36])[NH:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][CH:18]=1)[N:15]=[CH:14][N:13]=[C:12]2[NH:19][C:20]1[CH:25]=[CH:24][C:23]([O:26][CH2:27][C:28]2[CH:33]=[CH:32][CH:31]=[C:30]([F:34])[CH:29]=2)=[C:22]([Cl:35])[CH:21]=1.ClC1C=C(NC2C3C(=CC=C(N)C=3)N=CN=2)C=CC=1OCC1C=CC=C(F)C=1>>[Cl:35][C:22]1[CH:21]=[C:20]([NH:19][C:12]2[C:11]3[C:16](=[CH:17][CH:18]=[C:9]([NH:8][C:7]([CH:6]4[CH2:5][CH2:4][CH2:3][NH:37]4)=[O:36])[CH:10]=3)[N:15]=[CH:14][N:13]=2)[CH:25]=[CH:24][C:23]=1[O:26][CH2:27][C:28]1[CH:33]=[CH:32][CH:31]=[C:30]([F:34])[CH:29]=1Participants
3
Procedure
The procedure of (13-1) of Example 13 was repeated except for using 448 mg of the compound obtained in Example 15 instead of the compound obtained in Example 12 to obtain the title compound (297 mg, 82%).
Sources & evidence
- ORD record
- ord-5bbe020ed5804a1299e61d374e966283
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08003658B2
Reaction notes
Loading…