HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639668Generated: November 1, 2026
Dichloromethane → N-{5-[7-(1-Ethyl-propyl)-2,5-dimethylpyrazolo[1,5-a]pyrimidin-3-yl]-4-methyl-thiophen-2-yl}acetamide
https://huagongshe.com/reaction/1639668
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 3-(5-Nitro-3-methyl-thiophene-2-yl)-7-(1-ethyl-propyl)-2,5-dimethyl-pyrazolo[1,5-a]pyrimidine | HCID 66721128 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-{5-[7-(1-Ethyl-propyl)-2,5-dimethylpyrazolo[1,5-a]pyrimidin-3-yl]-4-methyl-thiophen-2-yl}acetamide | HCID 66721108 | 26% |
Reaction Steps
Dissolve 3-(5-nitro-3-methyl-thiophene-2-yl)-7-(1-ethyl-propyl)-2,5-dimethyl-pyrazolo[1,5-a]pyrimidine (0.33 g, 0.92 mmol) in THF (10 mL) with 10% palladium on carbon (0.10 g), degas with vacuum/hydrogen atmosphere flush (3×) and stir under a hydrogen atmosphere (55 psi) at room temperature for 3 h. Confirm the reaction is complete using TLC. Dilute the reaction with THF (50 mL) and filter through diatomaceous earth, followed by concentration to a crude orange oil (0.328 g). Dissolve the oil in dichloromethane (4 mL) and 1.0 M NaOH (1 mL). Add acetyl chloride (0.038 mL, 0.52 mmol) to the reaction and stir in a sealed reaction vessel at room temperature over the weekend. Dilute the reaction with dichloromethane (100 mL) and wash with water. Collect the organic phase, dry over anhydrous magnesium sulfate, filter, and concentrate to a red oil under reduced pressure. Purify the oil using flash chromatography, eluting with 100% hexane/0% (15% ethyl acetate/10% 7 N ammoniated methanol/75% hexane) to 0% hexane/100% (15% ethyl acetate/10% 7 N ammoniated methanol/75% hexane) in a step gradient of 10% increments to give a brown foam (0.048 g, 26%). ES/MS m/z 371.0 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110580B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-b7d6d0c45749436bb8ab466796bdac46 |
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| Source note | uspto-grants-2012_02 |
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