Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82319Generated: October 25, 2026

Dimethylformamide dimethyl acetal → Methyl imidazo[1,2-a]pyrimidine-6-carboxylate

https://huagongshe.com/reaction/82319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamide dimethyl acetalHCID 78373—
Reactant6-Bromoimidazo[1,2-a]pyrimidineHCID 26967622—
CatalystPalladium ChlorideHCID 24290—
CatalystBinap, (A+-)-HCID 634876—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductMethyl imidazo[1,2-a]pyrimidine-6-carboxylateHCID 4535673135%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 6-bromoimidazo[1,2-a]pyrimidine (1.17 g, 6 mmol), BINAP (18 mg, 0.06 mmol), PdCl2 (6 mg) in MeOH (30 mL) and triethylamine (1.8 mL) was heated to 80° C. under CO (50 psi) for 12 hours in DMF (97.5 mL). DMF-DMA (70.6 mL, 495.8 mmol) was added and the mixture heated to 130° C. for 12 hours. The mixture was filtered and concentrated to give methyl imidazo[1,2-a]pyrimidine-6-carboxylate (365 mg, 35%) as a yellow solid which was used in the next step without further purification. To a solution of methyl imidazo[1,2-a]pyrimidine-6-carboxylate (365 mg, 2.1 mmol) in methanol was added 1M aq. LiOH (9.0 mL) and the resulting mixture was stirred for 10 hours at room temperature. The pH was adjusted to 5-6 using aq. HCl and the whole mixture extracted with EtOAc (3×30 mL). The combined organic layers were dried over Na2SO4 and evaporated in vacuo to give the title compound as white solid in 39% yield, 133 mg

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846698B2
Source datasetuspto-grants-2014_09
ORD IDord-1f5f4c64fc574cdf9e146e557a0fc9c9
Source noteuspto-grants-2014_09