2-Methylpiperidine → HCID 11508283, compound

HRID 1445792Notes

Reaction equation

HRID 1445792 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][CH:10]=[C:11]([CH2:13]Cl)[N:12]=2)=[CH:4][CH:3]=1.[CH3:15][CH:16]1[CH2:21][CH2:20][CH2:19][CH2:18][NH:17]1>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][CH:10]=[C:11]([CH2:13][N:17]3[CH2:18][CH2:19][CH2:20][CH2:21][CH:16]3[CH3:15])[N:12]=2)=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 79742-MethylpiperidineHCID 155551142-(4-Bromophenyl)-4-(chloromethyl)oxazole2×

Product 1

HCID 11508283HCID 11508283, compound

Procedure

The titled compound is prepared substantially in accordance with the procedure of Example 16 using 2-(4-Bromo-phenyl)-4-chloromethyl-oxazole (See Intermediate 1) and 2-methylpiperidine. MS (m/e): 336.2 (M+1)

Sources & evidence

ORD record
ord-04376a78c17546f3a5af5614c7d564a2
Source dataset
uspto-grants-2010_02
Patent number
US07666871B2

Reaction notes

Loading…