HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40713Generated: October 30, 2026
Ethyl Acetate → HCID 15604198, compound
https://huagongshe.com/reaction/40713
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | (5-Amino-1H-pyrazol-4-yl)(thiophen-2-yl)methanone | HCID 11550150 | — |
| Reactant | N-[2-chloro-5-(3-dimethylamino-acryloyl)-phenyl]-N-methyl-methanesulfonamide | HCID 67279091 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 15604198 | HCID 15604198 | 73% |
Reaction Steps
A mixture of 0.076 g (0.39 mmol) of (5-amino-1H-pyrazol-4-yl)-thiophene-2-yl-methanone and 0.124 g (0.39 mmol) of (N-[2-chloro-5-(3-dimethylamino-acryloyl)-phenyl]-N-methyl-methanesulfonamide in 10 ml of glacial acetic acid was refluxed for 1.5 hours and then the solvent was removed by reduced pressure distillation. To the resulting residue were added 15 ml of dichloromethane and 10 ml of saturated sodium bicarbonate solution. The two layers were separated, and the aqueous layer was washed with 10 ml of dichloromethane. The organic layers were washed with 10 ml of water and dried over magnesium sulfate. The dichloromethane layer was evaporated to dryness to yield an oil which, in the presence of ethyl acetate, gave 128 mg of N-{2-chloro-5-[3-(thiophene-2-carbonyl)-pyrazolo[1,5-a]pyrimidin-7-yl]-phenyl}-N-methyl-methanesulfonamide as a solid (yield 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530482B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-dbbb60323e7244509be036ad9dd5071a |
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| Source note | uspto-grants-2013_09 |
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