4-Benzyloxyaniline → (4-Benzyloxy-phenyl)-(6-(5-methyl-1,3,4-oxadiazol-2-yl)-pyrido[3,4-d]pyrimidin-4yl)-amine

HRID 1532967Notes

Reaction equation

[CH2:1]([O:8][C:9]1[CH:15]=[CH:14][C:12]([NH2:13])=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl[C:17]1[C:18]2[CH:26]=[C:25]([C:27]3[O:28][C:29]([CH3:32])=[N:30][N:31]=3)[N:24]=[CH:23][C:19]=2[N:20]=[CH:21][N:22]=1>>[CH2:1]([O:8][C:9]1[CH:10]=[CH:11][C:12]([NH:13][C:17]2[C:18]3[CH:26]=[C:25]([C:27]4[O:28][C:29]([CH3:32])=[N:30][N:31]=4)[N:24]=[CH:23][C:19]=3[N:20]=[CH:21][N:22]=2)=[CH:14][CH:15]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

Reactant 2

HCID 228604-Benzyloxyaniline

HCID 22011950HCID 22011950, compound

Product 1

HCID 22011961(4-Benzyloxy-phenyl)-(6-(5-methyl-1,3,4-oxadiazol-2-yl)-pyrido[3,4-d]pyrimidin-4yl)-amine

Procedure

The title compound was prepared according to Procedure A from 4-benzyloxyaniline and 4-chloro-6-(5-methyl-1,3,4-oxadiazol-2-yl)pyrido[3,4-d]pyrimidine; δH [2H6]DMSO 11.33 (1H,s), 9.49 (1H,s), 9.39 (1H,s), 8.93 (1H,s), 7.80 (2H,d), 7.53 (2H,dd), 7.45 (3H,m), 7.20 (2H,d), 5.25 (2H,s), 2.75 (3H,s); m/z (M+1+) 411.

Sources & evidence

ORD record: ord-4ecdb397e82741508819fd730ee6c9cd
Source dataset: uspto-grants-2001_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06207669B1

Reaction notes

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