Phenethylamine → 3-(p-Tolyl)-1,4-dihydro-4-oxo-5-phenethylamino-1,6-naphthyridine

HRID 1044324Notes

Reaction equation

HRID 1044324 reaction equation
F[C:2](F)(F)[C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:18](=[O:19])[C:17]3[C:12](=[CH:13][CH:14]=[N:15][C:16]=3[NH:20]C3C=CC=CC=3)[NH:11][CH:10]=2)=[CH:5][CH:4]=1.Cl[C:30]1[CH:35]=[CH:34][C:33]([CH2:36][C:37](OCC)=O)=[CH:32][CH:31]=1.FC(F)(F)C1C=CC(CC(OCC)=O)=CC=1.C(N)CC1C=CC=CC=1.NC1C=CC=CC=1>>[C:3]1([CH3:2])[CH:8]=[CH:7][C:6]([C:9]2[C:18](=[O:19])[C:17]3[C:12](=[CH:13][CH:14]=[N:15][C:16]=3[NH:20][CH2:37][CH2:36][C:33]3[CH:34]=[CH:35][CH:30]=[CH:31][CH:32]=3)[NH:11][CH:10]=2)=[CH:5][CH:4]=1

Participants

6

Procedure

3-(4-Trifluoromethylphenyl)-1,4-dihydro-4-oxo-5-phenylamino-1,6-naphthyridine The title compound was prepared as described in Example 1 above except that ethyl (4-chlorophenyl)acetate was replaced with ethyl (4-trifluoromethyl-phenyl)acetate and phenethylamine was replaced with aniline. MS 382 (M+1)+.

Sources & evidence

ORD record
ord-c5f81447b6e24a9f87caca3400717fc8
Source dataset
uspto-grants-2013_10
Patent number
US08563579B2

Reaction notes

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