4-(2-(Piperidin-1-yl)ethoxy)benzaldehyde → HCID 178492969, compound

HRID 2218430Notes

Reaction equation

HRID 2218430 reaction equation
[Cl:1][C:2]1[C:3]([O:10][CH3:11])=[C:4]([NH2:9])[C:5]([NH2:8])=[N:6][CH:7]=1.[N:12]1([CH2:18][CH2:19][O:20][C:21]2[CH:28]=[CH:27][C:24]([CH:25]=O)=[CH:23][CH:22]=2)[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1>>[Cl:1][C:2]1[C:3]([O:10][CH3:11])=[C:4]2[N:9]=[C:25]([C:24]3[CH:23]=[CH:22][C:21]([O:20][CH2:19][CH2:18][N:12]4[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]4)=[CH:28][CH:27]=3)[NH:8][C:5]2=[N:6][CH:7]=1

Participants

3

Reactant 2

HCID 111838924-(2-(Piperidin-1-yl)ethoxy)benzaldehydeHCID 57482673HCID 57482673, compound

Product 1

HCID 178492969HCID 178492969, compound

Procedure

By a procedure similar to Example 269 but using 5-chloro-4-methoxypyridin-2,3-diamine and 4-(2-piperidin-1-ylethoxy)benzaldehyde, the title compound was obtained as the bis(trifluoroacetate).

Sources & evidence

ORD record
ord-d18fd4a6ecad4188acbbb8544e199c57
Source dataset
uspto-grants-2008_08
Patent number
US07410966B2

Reaction notes

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