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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878455Generated: November 1, 2026

Thiourea → HCID 44137768, compound

https://huagongshe.com/reaction/1878455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
ReactantHCID 44136066HCID 44136066—
SolventMethanolHCID 887—
ProductHCID 44137768HCID 4413776835.6%

Reaction Steps

To a suspension of 60 mg of crude 6-(2-bromoacetyl)-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in 10 mL of methanol are added 14 mg of thiourea. The reaction mixture is heated for 45 minutes at reflux and then concentrated to dryness under reduced pressure. The residue is chromatographed on a silica cartridge, eluting with a mixture of dichloromethane and methanol (gradient of from 100/0 to 90/10). The fractions containing the expected product are combined and evaporated to dryness under reduced pressure to give 20 mg of 6-(2-aminothiazol-4-yl)-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314109B2
Source datasetuspto-grants-2012_11
ORD IDord-a06b14e5496c4b789dd9539c6fed9843
Source noteuspto-grants-2012_11