Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 209907-25-5 | HCID 12602976 | — |
| Reactant | 4-Allylamino-2-chloro-6-nitroquinazoline | HCID 18326487 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 18326572 | HCID 18326572 | 80.9% |
Reaction Steps
150 mg (0.57 mmol) of 4-allylamino-2-chloro-6-nitroquinazoline was dissolved in 2 ml of acetonitrile, and 305 mg (2.83 mmol) of trans-2-butenylamine hydrochloride and 0.39 ml (2.83 mmol) of triethylamine were added thereto, followed by stirring at 50° C. for 6 hours. To the reaction solution was water added, 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 138 mg (yield: 80.9%) 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-2209ba33f2764431a12fe9c21fc2b7f4 |
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| Source note | uspto-grants-2002_01 |
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