2-Chloropyrimidine → HCID 23725966, compound

HRID 2219338Notes

Reaction equation

[F:1][C:2]1[CH:3]=[C:4]([C:8]2[C:12]([C:13]3[N:14]=[CH:15][NH:16][CH:17]=3)=[C:11]([CH3:18])[O:10][N:9]=2)[CH:5]=[CH:6][CH:7]=1.Cl[C:20]1[N:25]=[CH:24][CH:23]=[CH:22][N:21]=1>>[F:1][C:2]1[CH:3]=[C:4]([C:8]2[C:12]([C:13]3[N:14]=[CH:15][N:16]([C:20]4[N:25]=[CH:24][CH:23]=[CH:22][N:21]=4)[CH:17]=3)=[C:11]([CH3:18])[O:10][N:9]=2)[CH:5]=[CH:6][CH:7]=1

Participants

Reactant 2

HCID 744042-Chloropyrimidine

HCID 178434992HCID 178434992, compound

Product 1

HCID 23725966HCID 23725966, compoundYield 72%

Procedure

As described for Example 40, 3-(3-fluoro-phenyl)-4-(1H-imidazol-4-yl)-5-methyl-isoxazole (100 mg, 0.41 mmol) using 2-chloropyrimidine instead of 4-fluoroacetophenone was converted to the title compound (95 mg, 72%) which was obtained as an off-white solid. MS: m/e=322.4 [M+H]+.

Sources & evidence

ORD record: ord-4f3952f846354cbd9188af06ec15fb8d
Source dataset: uspto-grants-2008_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07414061B2

Reaction notes

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