HCID 12088101, compound → HCID 12088109, compound

HRID 1168249Notes

Reaction equation

HRID 1168249 reaction equation
[CH2:1]([N:5]1[CH2:10][CH2:9][CH:8]([CH2:11][NH:12][C:13]([C:15]2[C:16]3[N:17]([CH:24]=[CH:25][N:26]=3)[C:18]([NH:22][CH3:23])=[C:19]([Cl:21])[CH:20]=2)=[O:14])[CH2:7][CH2:6]1)[CH2:2][CH2:3]C.[CH3:27][O:28]CCCN1CCC(CN)CC1>>[Cl:21][C:19]1[CH:20]=[C:15]([C:13]([NH:12][CH2:11][CH:8]2[CH2:9][CH2:10][N:5]([CH2:1][CH2:2][CH2:3][O:28][CH3:27])[CH2:6][CH2:7]2)=[O:14])[C:16]2[N:17]([CH:24]=[CH:25][N:26]=2)[C:18]=1[NH:22][CH3:23]

Participants

3

Reactant 2

HCID 12088101HCID 12088101, compoundHCID 12088108HCID 12088108, compound

Product 1

HCID 12088109HCID 12088109, compound

Procedure

The title compound was prepared, according to the procedure described in the step 3 of EXAMPLE 5, from 6-chloro-5-(methylamino)imidazo[1,2-a]pyridine-8-carboxylic acid hydrochloride (EXAMPLE 8, Step 4) and {1-[3-(methyloxy)propyl]-4-piperidinyl}methylamine (EXAMPLE 7, Step 2).

Sources & evidence

ORD record
ord-86afabcb079a43feae3e45c65ae44190
Source dataset
uspto-grants-2003_09
Patent number
US06624162B2

Reaction notes

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