Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382735Generated: November 2, 2026

4-chloro-1-methyl-1H-pyrazole-5-carboxylic acid → HCID 51035029, compound

https://huagongshe.com/reaction/2382735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-chloro-1-methyl-1H-pyrazole-5-carboxylic acidHCID 670823—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant5-Morpholin-4-yl-2-phenyl-imidazo[1,2-c]pyrimidin-7-ylamineHCID 67041977—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 51035029HCID 510350291.5%

Reaction Steps

Under an atmosphere of nitrogen, N—N-diisopropylethylamine (121 mg) and 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TBTU, 120 mg) were added to a solution of 4-chloro-2-methyl-2H-pyrazole-3-carboxylic acid (50 mg, 0.31 mmol, Art-Chem B000148) in DMF (3 ml). After 30 min, 5-morpholin-4-yl-2-phenyl-imidazo[1,2-c]pyrimidin-7-ylamine (110 mg, 0.37 mmol) was added, and the black solution was stirred at r.t. overnight. The reaction mixture was taken up in ethyl acetate and washed with water. After drying (Na2SO4), the solvent was evaporated and the title compound (2 mg, 1.1%) was isolated by preparative, inverse-phase HPLC (Agilent Zorbax XdB-C18 column, time per run ˜7 min, flow rate 30 ml/min, solvent gradient H2O/CH3CN=95:5-5:95). MS (m/e)=438.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263584B2
Source datasetuspto-grants-2012_09
ORD IDord-c7be7f5e5af44db49859392eed766748
Source noteuspto-grants-2012_09