2-Aminopyridine → HCID 71087665, compound

HRID 927372Notes

Reaction equation

[Cl:1][C:2]1[CH:3]=[C:4]([C:8]2[N:13]=[C:12]([C:14]([OH:16])=O)[CH:11]=[CH:10][CH:9]=2)[CH:5]=[CH:6][CH:7]=1.[N:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[NH2:23]>>[N:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[NH:23][C:14]([C:12]1[CH:11]=[CH:10][CH:9]=[C:8]([C:4]2[CH:5]=[CH:6][CH:7]=[C:2]([Cl:1])[CH:3]=2)[N:13]=1)=[O:16]

Participants

Reactant 2

HCID 104392-Aminopyridine

HCID 247301356-(3-Chlorophenyl)picolinic acid

Product 1

HCID 71087665HCID 71087665, compound

Procedure

The title compound was synthesized in analogy to Example 1, using 6-(3-chlorophenyl)-2-pyridinecarboxylic acid (CAN 863704-38-5) and 2-pyridinamine (CAN 504-29-0) as starting materials, MS (D) m/e: 310.0 [M+H]+.

Sources & evidence

ORD record: ord-00ae9f197dc64ec79bb067c2506e55cc
Source dataset: uspto-grants-2016_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09290451B2

Reaction notes

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