4-(N-Boc-amino)piperidine → HCID 59553128, compound

HRID 1171287Notes

Reaction equation

HRID 1171287 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:29]=[C:30]([N:32]2[CH2:37][CH2:36][O:35][CH2:34][CH2:33]2)[CH:31]=1)[C:5]([NH:7][C:8]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[C:11]([O:18][C:19]2[CH:24]=[CH:23][N:22]=[C:21](S(C)(=O)=O)[N:20]=2)=[CH:10][CH:9]=1)=[O:6].[C:38]([O:42][C:43](=[O:51])[NH:44][CH:45]1[CH2:50][CH2:49][NH:48][CH2:47][CH2:46]1)([CH3:41])([CH3:40])[CH3:39]>>[C:38]([O:42][C:43](=[O:51])[NH:44][CH:45]1[CH2:50][CH2:49][N:48]([C:21]2[N:20]=[C:19]([O:18][C:11]3[C:12]4[C:17](=[CH:16][CH:15]=[CH:14][CH:13]=4)[C:8]([NH:7][C:5](=[O:6])[C:4]4[CH:29]=[C:30]([N:32]5[CH2:37][CH2:36][O:35][CH2:34][CH2:33]5)[CH:31]=[C:2]([F:1])[CH:3]=4)=[CH:9][CH:10]=3)[CH:24]=[CH:23][N:22]=2)[CH2:47][CH2:46]1)([CH3:41])([CH3:39])[CH3:40]

Participants

3

Reactant 2

HCID 7238334-(N-Boc-amino)piperidineHCID 595530953-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamide

Product 1

HCID 59553128HCID 59553128, compound

Procedure

Compound is prepared from 3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamide and piperidin-4-yl-carbamic acid t-butyl ester according to conditions described in general procedure C. Mp: 214-216° C.; 1H NMR (400 MHz, DMSO-d6) δ 1.33-1.41 (m, 14 H), 2.47-3.41 (m, 4H), 3.25-3.28 (m, 4H), 3.75-3.78 (m, 4 H), 4.20 (s, 1 H), 6.20 (d, J=5.5 Hz, 1H), 6.77-6.79 (m, 1 H), 7.00-7.05 (m, 1H), 7.18-7.26 (m, 1H), 7.38-7.63 (m, 5H), 7.85 (d, J=9.2 Hz, 1H), 8.00 (d, J=8.4 Hz, 1H), 8.26 (d, J=5.5 Hz, 1H), 10.47 (s, 1H).

Sources & evidence

ORD record
ord-12131a27a1824cd09ab402f04a87d0c4
Source dataset
uspto-grants-2010_11
Patent number
US07829560B2

Reaction notes

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