HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448135Generated: October 30, 2026
2,4,6-Trimethylpyridine → 5-tert-butyl 1-ethyl 3-[(4-chloromethyl-benzoyl)amino]-1H-thieno[2,3-c]pyrazole-1,5-dicarboxylate
https://huagongshe.com/reaction/448135
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Reactant | 4-(Chloromethyl)benzoyl chloride | HCID 70136 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | tert-butyl 3-amino-1H-thieno[2,3-c]pyrazole-5-carboxylate | HCID 178450636 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-tert-butyl 1-ethyl 3-[(4-chloromethyl-benzoyl)amino]-1H-thieno[2,3-c]pyrazole-1,5-dicarboxylate | HCID 66785832 | — |
Reaction Steps
4-Chloromethylbenzoyl chloride (5.42 g 28.7 mmol) was added to a suspension of tert-butyl 3-amino-1H-thieno[2,3-c]pyrazole-5-carboxylate (5.94 g, 19.1 mmol) in dry DCM (150 mL) and 2,4,6-collidine (6.94 g, 57.3 mmol) under stirring at 20° C. The resulting suspension was stirred for 3 hours at room temperature. 300 mL of aqueous sodium bicarbonate were then added to the reaction mixture and the organic layer was separated, washed with brine, dried over sodium sulphate and evaporated. The residue was triturated with hexane, filtered and dried at 40° C. under vacuum to give 8.3 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481584B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-902743747b524328829a742c8cca5b3a |
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| Source note | uspto-grants-2013_07 |
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