Isonicotinic Acid → HCID 56961775, compound

HRID 1958112Notes

Reaction equation

HRID 1958112 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]=[C:10]([NH2:19])[CH:11]=[N:12][C:13]=2[O:14][CH2:15][CH:16]2[CH2:18][CH2:17]2)=[CH:4][CH:3]=1.[C:20](O)(=[O:27])[C:21]1[CH:26]=[CH:25][N:24]=[CH:23][CH:22]=1>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]=[C:10]([NH:19][C:20](=[O:27])[C:21]3[CH:26]=[CH:25][N:24]=[CH:23][CH:22]=3)[CH:11]=[N:12][C:13]=2[O:14][CH2:15][CH:16]2[CH2:18][CH2:17]2)=[CH:4][CH:3]=1

Participants

3

Procedure

The title compound was synthesized in analogy to Example 1, using 5-(4-chloro-phenyl)-6-cyclopropylmethoxy-pyridin-3-ylamine and isonicotinic acid as starting materials, MS (LC/MS): 380.2 (M+H).

Sources & evidence

ORD record
ord-5bb358a6015f480cb4c0b6a0aec0cfb8
Source dataset
uspto-grants-2013_04
Patent number
US08410107B2

Reaction notes

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