HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250597Generated: November 3, 2026
1,1-Dimethylhydrazine → HCID 18326472, compound
https://huagongshe.com/reaction/1250597
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1-Dimethylhydrazine | HCID 5976 | — |
| Reactant | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 6-Nitro-2,4(1H,3H)-quinazolinedione | HCID 816982 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18326472 | HCID 18326472 | — |
Reaction Steps
To 300 mg (1.45 mmol) of 6-nitroquinazoline-2,4(1H,3H)-dione were added 1 ml of 1,3-dimethyl-2-imidazolidinone and 1.23 g (8.05 mmol) of phosphorus oxychloride, and the resulting mixture was subjected to heating under reflux for 3 hours. After phosphorus oxychloride was removed in vacuo, the mixture was dissolved in 3 ml of acetonitrile, followed by addition of 520 mg (8.69 mmol) of N,N-dimethylhydrazine and stirring under ice cooling for 30 minutes. To the reaction solution was added water, followed by extraction with ethyl acetate, washing with brine and drying over anhydrous sodium sulfate. After the solvent was distilled off to give 2-chloro-4-(2,2-dimethylhydrazino)-6-nitroquinazoline. After 2.00 ml (26.65 mmol) of allylamine was added thereto and then the mixture was stirred at room temperature for 3 hours, water was added to the reaction solution, followed by extraction with ethyl acetate, washing with brine and drying over anhydrous sodium sulfate. After the solvent was distilled off, the residue was purified by a silica gel column to give 73 mg (17.5%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06339089B2 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-784c7475af9548e391af77f290d69c49 |
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| Source note | uspto-grants-2002_01 |
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