HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102444Generated: October 30, 2026
Potassium Carbonate → HCID 86604092, compound
https://huagongshe.com/reaction/2102444
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-butyl (3aR,5r,6aS)-5-(((methylsulfonyl)oxy)methyl)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate | HCID 86604091 | — |
| Reactant | HCID 136335142 | HCID 136335142 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 86604092 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576074B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-9cc45868e9fa4f32bc5436adb9645d75 |
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| Source note | uspto-grants-2009_08 |
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