2-(4-(4-Fluorobenzoyl)piperidin-1-YL)acetic acid → HCID 136237383, compound
Reaction equation
[C@@H:1]([NH:5][CH2:6][C:7]1[NH:8][C:9](=[O:17])[C:10]2[CH2:16][O:15][CH2:14][CH2:13][C:11]=2[N:12]=1)([CH2:3][CH3:4])[CH3:2].[F:18][C:19]1[CH:36]=[CH:35][C:22]([C:23]([CH:25]2[CH2:30][CH2:29][N:28]([CH2:31][C:32](O)=[O:33])[CH2:27][CH2:26]2)=[O:24])=[CH:21][CH:20]=1>>[C@@H:1]([N:5]([CH2:6][C:7]1[NH:8][C:9](=[O:17])[C:10]2[CH2:16][O:15][CH2:14][CH2:13][C:11]=2[N:12]=1)[C:32](=[O:33])[CH2:31][N:28]1[CH2:29][CH2:30][CH:25]([C:23](=[O:24])[C:22]2[CH:21]=[CH:20][C:19]([F:18])=[CH:36][CH:35]=2)[CH2:26][CH2:27]1)([CH2:3][CH3:4])[CH3:2]Participants
3
Procedure
Following general procedure of Example 4, the title compound was prepared (8.7 mg) from (S)-2-((sec-butylamino)methyl)-7,8-dihydro-3H-pyrano[4,3-d]pyrimidin-4(5H)-one and 2-(4-(4-fluorobenzoyl)piperidin-1-yl)acetic acid. Exact mass calculated for C26H33FN4O4 484.6. found 485.4 (ESI, M+H); 1H NMR (400 MHz, dichloromethane-d2) δ ppm 7.87-8.08 (m, 2H) 7.09-7.25 (m, 2H) 4.41-4.57 (m, 2H) 4.20-4.40 (m, 3H) 4.16 (d, J=8.08 Hz, 1H) 3.83-3.97 (m, 2H) 3.19-3.42 (m, 3H) 3.11 (d, J=5.56 Hz, 1H) 2.93 (d, J=8.59 Hz, 1H) 2.43-2.71 (m, 3H) 2.17-2.36 (m, 2H) 2.00 (br. s., 1H) 1.68-1.92 (m, 3H) 1.22 (d, J=6.57 Hz, 2H) 1.09 (d, J=7.07 Hz, 1H) 0.66-0.83 (m, 3H).
Sources & evidence
- ORD record
- ord-8a37d8b5a36541ceacca9ee2449e09b5
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09181266B2
Reaction notes
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