HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367219Generated: October 30, 2026
Dimethylformamide → HCID 178518115, compound
https://huagongshe.com/reaction/367219
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 23287612 | HCID 23287612 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178518115 | HCID 178518115 | 35.1% |
Reaction Steps
A mixture of 74 mg (0.23 mmol) of 2-[N-(4-chlorophenyl)-N-(4-oxo-4H-pyrido[3,2-e]-1,3-thiazin-2-yl]amino]acetonitrile and 1 ml of DMF was put in a 20 ml flask. To the mixture were then added 146 mg of sodium azide and 120 mg of ammonium chloride with stirring. The mixture was then stirred at a temperature of 120° C. for 4 hours. The resulting reaction mixture was allowed to cool, poured into water, and then extracted with ethyl acetate. The resulting organic phase was separated, washed with water and saturated brine, and then dried over sodium sulfate. The drying agent was then removed by filtration. The filtrate was then concentrated under reduced pressure. The resulting residue was then washed with cold ethanol to obtain 30 mg of 2-[N-(4-chlorophenyl)-N-(1H-tetrazol-5-ylmethyl)amino]-4H-pyrido[3,2-e]-1,3-thiazin-4-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06133258 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-33b1433787be464ea916c580e2da32b5 |
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| Source note | uspto-grants-2000_10 |
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