HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098094Generated: October 31, 2026
Chlorosuccinimide → 8-Chlorothieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine
https://huagongshe.com/reaction/2098094
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Thieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine | HCID 12226522 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 8-Chlorothieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine | HCID 68783490 | — |
Reaction Steps
To a stirring mixture of thieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine (123 mg, 0.7 mmol) in HOAc (1 mL) was added NCS (200 mg, 1.5 mmol), Pd(OAc)2 (48 mg, 0.21 mmol). The reaction mixture was stirred at 120° C. overnight. The reaction was neutralized with a saturated NaHCO3 solution and extracted with DCM. This product was purified via an isco column to give 8-chlorothieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine as the major product. Retention time (min)=1.663, method [1], MS (ESI) 211.0 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450363B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-ac6b56ded5f64c42ba865840db001697 |
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| Source note | uspto-grants-2013_05 |
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