HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069007Generated: October 27, 2026
N,N-Diisopropylmethylamine → 4-Methoxy-but-2-enoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amide
https://huagongshe.com/reaction/1069007
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Diisopropylmethylamine | HCID 547370 | — |
| Reactant | N4-(3-Bromophenyl)quinazoline-4,6-diamine | HCID 5328042 | — |
| Reactant | 4-Methoxycrotonyl chloride | HCID 22466554 | — |
| Reactant | Sodium hydrogencarbonate brine | HCID 129703874 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Methoxy-but-2-enoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amide | HCID 54391946 | 95.3% |
Reaction Steps
To a stirred solution of 1.0 g of N-(3-bromophenyl)-4,6-quinazolindiamine and 0.62 g of diisopropyl methylamine in 21 mL of tetrahydrofuran at 0° C. was added 0.62 g of 4-methoxycrotonyl chloride. The mixture was stirred at 0° C. for 1.5 hr and 10 min at room temperature. The mixture was poured into saturated sodium bicarbonate-brine and extracted with ethyl acetate. The organic solution was dried over magnesium sulfate. The solution was filtered through silica gel and the solvent was removed. The residue was recrystallized from 1-butanol to give 1.25 g of 4-Methoxy-but-2-enoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amide as a yellow solid: mass spectrum (m/e): M+H 415.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06251912B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-140e71bc53c54d56aec6bd1923a12126 |
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| Source note | uspto-grants-2001_06 |
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