HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → N-(4-((3-bromophenyl)amino)-6-quinazolinyl)-2-butynamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 2-Butynoic acid | HCID 68535 | — |
| Reactant | N4-(3-Bromophenyl)quinazoline-4,6-diamine | HCID 5328042 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-((3-bromophenyl)amino)-6-quinazolinyl)-2-butynamide | HCID 2776 | 55.3% |
Reaction Steps
A solution of 0.50 g of 2-butynoic acid in 10 ml of tetrahydrofuran was cooled in an ice bath. A 0.79 ml portion of isobutyl chloroformate followed by a 0.66 ml portion of N-methyl morpholine were added. After about 1 minute a solution of 1.6 g of N-(3-bromophenyl)-4,6-quinazolindiamine in 10 ml of pyridine was added. The reaction was allowed to come to room temperature and stir overnight. The solvents were removed at reduced pressure and the solid was recrystallized from n-butanol to give 1.07 g of N-[4-[(3-bromophenyl)amino]-6-quinazolinyl)-2-butynamide: mass spectrum (m/e): 381, 383.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06323209B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-be17a86decdd4ca89b9aee296451dc21 |
| Source note | uspto-grants-2001_11 |