6,6-Dimethyl-2-phenyl-piperidin-3-ylamine → HCID 21931794, compound

HRID 1244082Notes

Reaction equation

HRID 1244082 reaction equation
[CH3:1][C:2]1([CH3:15])[NH:7][CH:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:5]([NH2:14])[CH2:4][CH2:3]1.[CH3:16][O:17][C:18]1[CH:19]=[C:20]2[C:25](=[CH:26][C:27]=1[CH:28]=O)[N:24]([CH3:30])[C:23](=[O:31])[CH2:22][CH2:21]2>>[CH3:1][C:2]1([CH3:15])[NH:7][CH:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:5]([NH:14][CH2:28][C:27]2[CH:26]=[C:25]3[C:20]([CH2:21][CH2:22][C:23](=[O:31])[N:24]3[CH3:30])=[CH:19][C:18]=2[O:17][CH3:16])[CH2:4][CH2:3]1

Participants

3

Reactant 2

HCID 99644056,6-Dimethyl-2-phenyl-piperidin-3-ylamineHCID 101251786-Methoxy-1-methyl-2-oxo-1,2,3,4-tetrahydroquinoline-7-carbaldehyde

Product 1

HCID 21931794HCID 21931794, compound

Procedure

By a procedure similar to the previous examples 9 and 9A: prepared through the reaction of 6,6-dimethyl-2-phenyl-piperidin-3-ylamine with 6-Methoxy-1-methyl-2-oxo-1,2,3,4-tetrahydro-quinoline-7-carbaldehyde. Mass spectrum calcd for C25H34N3O2 (M+1) 408; found 408.

Sources & evidence

ORD record
ord-67e6dee9a8e74dd597dd98071291d030
Source dataset
uspto-grants-2006_10
Patent number
US07119207B2

Reaction notes

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