HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914838Generated: November 2, 2026
Phenylacetyl chloride → HCID 58034449, compound
https://huagongshe.com/reaction/1914838
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | methyl 7-amino-2-methylpyrazolo[1,5-a]pyrimidine-6-carboxylate | HCID 2763438 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58034449 | HCID 58034449 | — |
Reaction Steps
A 250 mL round-bottomed flask containing methyl 7-amino-2-methylpyrazolo[1,5-a]pyrimidine-6-carboxylate (1.10 g, 5.0 mmol, 1 eq.), CH2Cl2 (40 mL), and Et3N (2.04 g, 20 mmol, 4 eq.) was added slowly phenylacetyl chloride (6.16 g, 40 mmol, 8 eq.). Then the mixture was heated at 80° C. for 4 h. The mixture was allowed to cool and the solvent was removed in vacuo. The residue was dissolved in CH2Cl2 (40 mL) and water (25 mL). The aqueous phase was extracted with CH2Cl2 (2×15 mL). The combined organic solution was dried over Na2SO4. After filtration and concentration, the residue was purified by silica gel chromatography using MeOH and CH2Cl2 as the mobile phases to furnish Compound (20-1) as a yellowish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614221B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-e4319567ddcb4d98bb752bf998e86d7b |
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| Source note | uspto-grants-2013_12 |
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