2-(4-(4-Fluorobenzoyl)piperidin-1-YL)acetic acid → HCID 136219321, compound
Reaction equation
[CH2:1]([NH:4][CH2:5][C:6]1[NH:7][C:8](=[O:16])[C:9]2[CH2:15][O:14][CH2:13][CH2:12][C:10]=2[N:11]=1)[CH2:2][CH3:3].[F:17][C:18]1[CH:35]=[CH:34][C:21]([C:22]([CH:24]2[CH2:29][CH2:28][N:27]([CH2:30][C:31](O)=[O:32])[CH2:26][CH2:25]2)=[O:23])=[CH:20][CH:19]=1>>[F:17][C:18]1[CH:19]=[CH:20][C:21]([C:22]([CH:24]2[CH2:25][CH2:26][N:27]([CH2:30][C:31]([N:4]([CH2:5][C:6]3[NH:7][C:8](=[O:16])[C:9]4[CH2:15][O:14][CH2:13][CH2:12][C:10]=4[N:11]=3)[CH2:1][CH2:2][CH3:3])=[O:32])[CH2:28][CH2:29]2)=[O:23])=[CH:34][CH:35]=1Participants
3
Procedure
Following general procedure of Example 4, the title compound was prepared (37.3 mg) from 2-((propylamino)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 C25H31FN4O4 470.5. found 471.6 (ESI, M+H); 1H NMR (400 MHz, dichloromethane-d2) δ ppm 7.89-8.08 (m, 2H) 7.19 (t, J=8.34 Hz, 2H) 4.60 (s, 2H) 4.42-4.57 (m, 2H) 4.27 (br. s., 2H) 3.85-4.01 (m, 3H) 3.81 (br. s., 1H) 3.57 (br. s., 1H) 3.39 (br. s., 1H) 3.31 (br. s., 2H) 3.12-3.28 (m, 1H) 2.72 (br. s., 1H) 2.13 (s, 4H) 1.58-1.80 (m, 1H) 1.40-1.58 (m, 1H) 0.76-1.00 (m, 3H).
Sources & evidence
- ORD record
- ord-07fefb40a3df40d6a1a837db446674f0
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09181266B2
Reaction notes
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