Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102444Generated: October 30, 2026

Potassium Carbonate → HCID 86604092, compound

https://huagongshe.com/reaction/2102444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-butyl (3aR,5r,6aS)-5-(((methylsulfonyl)oxy)methyl)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylateHCID 86604091—
ReactantHCID 136335142HCID 136335142—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductHCID 86604092HCID 86604092—

Reaction Steps

A solution of 4-[(3,4-dichloro-2-fluorophenyl)amino]-6-(methyloxy)quinazolin-7-ol trifluoroacetate (salt) (0.22 g, 0.47 mmol), 1,1-dimethylethyl (3aR,6aS)-5-{[(methylsulfonyl)oxy]methyl}hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate (0.16 g, 0.51 mmol), K2CO3 (0.33 g, 2.36 mmol) in N,N-dimethylacetamide (5 mL) was heated in a sealed reaction tube at 90° C. for 12 h. The crude reaction mixture was diluted with 100 mL 10% methanol in ethyl acetate and washed with saturated aqueous sodium bicarbonate (1×30 mL), water (1×30 mL) and brine (1×30 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. Column chromatography (SiO2, 3:2 hexanes:acetone) provided 1,1-dimethylethyl (3aR,6aS)-5-({[4-[(3,4-dichloro-2-fluorophenyl)amino]-6-(methyloxy)quinazolin-7-yl]oxymethyl) hexahydrocyclopenta-[c]pyrrole-2(1H)-carboxylate which was used directly in the next step. MS (EI) for C28H31Cl2FN4O4: 577, 579 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576074B2
Source datasetuspto-grants-2009_08
ORD IDord-9cc45868e9fa4f32bc5436adb9645d75
Source noteuspto-grants-2009_08