HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250582Generated: October 25, 2026
Isopropylamine → 2-Chloro-4-isopropylamino-6-nitroquinazoline
https://huagongshe.com/reaction/1250582
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | N,N-bis(1-methylethyl)formamide | HCID 75912 | — |
| Reactant | 6-Nitro-2,4(1H,3H)-quinazolinedione | HCID 816982 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-4-isopropylamino-6-nitroquinazoline | HCID 18326428 | 67.5% |
Reaction Steps
To 1.00 g (4.83 mmol) of 6-nitroquinazoline-2,4 (1H,3H)-dione were added 32.90 g (0.22 mol) of phosphorus oxychloride and 0.70 ml (4.83 mmol) of diisopropylformamide, and the resulting mixture was subjected to heating under reflux for 24 hours. After phosphorus oxychloride was removed in vacuo, the mixture was dissolved in 15 ml of acetonitrile, followed by addition of 2.49 ml (29.11 mmol) of isopropylamine under ice cooling 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, the residue was purified by a silica gel column to give 870 mg (yield: 67.5%) 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-f116485c5cf24fc8b6a0f56ed644b8b4 |
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| Source note | uspto-grants-2002_01 |
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