HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250601Generated: October 27, 2026
Tert-Butylamine → 4-t-Butylamino-2-chloro-6-nitroquinazoline
https://huagongshe.com/reaction/1250601
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| 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 | 4-t-Butylamino-2-chloro-6-nitroquinazoline | HCID 18326506 | 64.2% |
Reaction Steps
To 250 mg (1.21 mmol) of 6-nitroquinazoline-2,4(1H,3H)-dione were added 5.00 ml (53.64 mmol) of phosphorus oxychloride and 0.18 ml (1.21 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 5 ml of acetonitrile, followed by addition of 1.26 ml (12.10 mmol) of t-butylamine 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 218 mg (64.2%) 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-27d5da839434492eacac3aa1683bc395 |
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| Source note | uspto-grants-2002_01 |
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