HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542964Generated: October 29, 2026
Hydrochloric Acid → 2,4-Diamino-5-(4-azido-3,5-dimethoxy-benzyl)pyrimidine
https://huagongshe.com/reaction/542964
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2,4-Diamino-5-(4-amino-3,5-dimethoxy-benzyl)pyrimidine dihydrochloride | HCID 21280986 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,4-Diamino-5-(4-azido-3,5-dimethoxy-benzyl)pyrimidine | HCID 21280945 | — |
Reaction Steps
A solution of 7 g. of 2,4-diamino-5-(4-amino-3,5-dimethoxy-benzyl)-pyrimidine dihydrochloride in 60 ml. of 1N hydrochloric acid and 40 ml. of water was treated over a period of 5 minutes with stirring and ice-cooling with a solution of 1.52 g. of sodium nitrite in 10 ml. of water. After stirring at 0° C. for 30 minutes, a solution of 1.43 g. of sodium azide in 20 ml. of water was added. The solution was stirred at 0° C. for 2 hours and then treated with sodium bicarbonate to obtain an alkaline reaction. After stirring at 0° C. for 1 hour, the precipitate was removed by filtration with suction, washed with water and recrystallized from methanol, whereby there was obtained 2,4-diamino-5-(4-azido-3,5-dimethoxy-benzyl)-pyrimidine having a melting point of 152° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04659818 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-8be0f7f08f52429fb7c3d546637b9f8f |
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| Source note | uspto-grants-1987_04 |
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