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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392980Generated: October 27, 2026

4-Bromo-4'-methylbenzophenone → HCID 10272637, compound

https://huagongshe.com/reaction/1392980

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-4'-methylbenzophenoneHCID 2757056—
Reactant4-(Imidazo[1,2-a]pyridin-3-yl)pyrimidin-2-amineHCID 69197864—
ProductHCID 10272637HCID 1027263717%

Reaction Steps

The title compound was prepared from 2-amino-4-(imidazo[1,2-a]pyridin-3-yl)pyrimidine and 4-bromo4′-methylbenzophenone following the general method of Example 2. The crude product was purified by column chromatography on silica gel using chloroform/ethanol, 98:2, as the eluent affording 52 mg (17% yield) of the title compound as a yellow solid: mp 238.9-239.2° C.; 1H NMR (400 MHz, DMSO-d6) δ 10.15-10.13 (m, 2 H), 8.64 (s, 1 H), 8.50 (d, J=5.3 Hz, 1 H), 7.96 (d, J=8.5 Hz, 2 H), 7.79-7.74 (m, 3 H), 7.63 (d, J=7.8 Hz, 2 H), 7.53-7.49 (m, 2 H), 7.35 (d, J=7.7 Hz, 2 H), 7.16 (t, J=6.8 Hz, 1 H), 2.40 (s, 3 H); 13C NMR (400 MHz, DMSO-d6) δ 194.4, 159.4, 157.7, 157.4, 148.4, 145.1, 142.7, 139.4, 135.5, 131.5, 130.1, 129.9, 129.8, 129.3, 127.5, 121.3, 118.2, 117.8, 114.2, 108.6, 21.5; MS (TSP) m/z 406 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345050B2
Source datasetuspto-grants-2008_03
ORD IDord-48008c41dd20405cb0529cd9a52265a1
Source noteuspto-grants-2008_03