4-Aminopyridine → HCID 15082702, compound

HRID 272755Notes

Reaction equation

HRID 272755 reaction equation
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:8][C:9]1[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][C:10]=1[O:16][CH3:17].NC1C=CN=CC=1>>[Cl:15][C:12]1[CH:13]=[CH:14][C:9]([NH:8][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[C:10]([O:16][CH3:17])[CH:11]=1

Participants

4

Reactant 3

HCID 17274-AminopyridineHCID 7143Benzenamine, 4-chloro-2-methoxy-HCID 7961Bromobenzene

Product 1

HCID 15082702HCID 15082702, compound

Procedure

The title compound was prepared by substituting bromobenzene and 2-amino-5-chloroanisole for Example 189A and 4-aminopyridine, respectively, in Example 191. MS (ESI) m/e 234 (M+H)+.

Sources & evidence

ORD record
ord-6b693648cf6548a08944f63437530862
Source dataset
uspto-grants-2008_11
Patent number
US07456169B2

Reaction notes

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