HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904550Generated: October 29, 2026
Hydrochloric Acid → HCID 178422273, compound
https://huagongshe.com/reaction/904550
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 2-methyl-10-oxo-10H-pyrido[1,2-a]thieno[3,2-d]pyrimidine-7-carbonitrile | HCID 12953055 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178422273 | HCID 178422273 | 80.9% |
Reaction Steps
A mixture of 0.21 g (0.00087 mol) of 2-methyl-10-oxo-10H-pyrido[1,2-a]thieno[3,2-d]pyrimidine-7-carbonitrile (Example 45), 0.2 g (0.0031 mol) of sodium azide and 0.166 g (0.0031 mol) of ammonium chloride in 50 ml of dimethylformamide is stirred and heated to 100° C. for twenty-four hours. The reaction mixture is cooled, poured into 900 ml of ice water and acidified with concentrated hydrochloric acid. The resulting precipitate is filtered to give 0.2 g of 2-methyl-7-(1H-tetrazol-5-yl)-10H-pyrido[1,2-a]thieno[3,2-d]pyrimidin-10-one; mp 321°-325° C. (dec) after recrystallization from pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04230707 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-cc20a00f5300475fb04ce9993abcb458 |
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| Source note | uspto-grants-1980_10 |
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