HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250612Generated: November 3, 2026
1,3-Dimethyl-2-imidazolidinone → HCID 54459706, compound
https://huagongshe.com/reaction/1250612
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 6-Nitro-2,4(1H,3H)-quinazolinedione | HCID 816982 | — |
| Reactant | BUT-3-EN-2-AMINE HCL | HCID 18185425 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54459706 | HCID 54459706 | — |
Reaction Steps
To 278 mg (1.45 mmol) of 6-nitroquinazoline-2,4(1H,3H)-dione were added 0.71 ml of 1,3-dimethyl-2-imidazolidinone and 5.48 g (35.76 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 2.81 ml (20.07 mmol) of triethylamine and 281 mg (2.61 mmol) of 1-methyl-2-propenylamine hydrochloride and stirring under ice cooling for 2 hours. 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-(1-methyl-2-propenylamino)-6-nitroquinazoline. After 1.00 ml (10.12 mmol) of n-butylamine 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 (17.3%) 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-ae2cc88b4ba04e1c91dcbef892969cc1 |
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| Source note | uspto-grants-2002_01 |
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