HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098095Generated: October 30, 2026
8-Chlorothieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine → HCID 178509328, compound
https://huagongshe.com/reaction/2098095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 8-Chlorothieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine | HCID 68783490 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178509328 | HCID 178509328 | — |
Reaction Steps
To a stirring mixture of 8-chlorothieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine (60 mg, 0.285 mmol) in MeOH (10 mL) was added N-methylethyl 1,2-diamine (106 mg, 1.4 mmol). The resulting mixture was warmed to 60° C. for 1 hr. The reaction mixture was cooled to rt and then diluted with DCM. This mixture was then washed several times with a saturated NH4Cl solution. The organic layer was dried over MgSO4, filtered, and concentrated under reduced pressure to give 5-chloro-3-(4H-1,2,4-triazol-3-yl)thiophen-2-amine. This amine was taken directly to the next coupling reaction without further purification. Retention time (min)=1.227, method [1], MS (ESI) 201.1 (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-b601b6b4440c452a9f273182f0adf02a |
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| Source note | uspto-grants-2013_05 |
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