HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → [4-Chloro-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 | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Chloroquinazolin-6-amine | HCID 18350691 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | [4-Chloro-6-quinazolinyl]-2-butynamide | HCID 54436052 | — |
Reaction Steps
A solution of 1.64 g of 2-butynoic acid in 46 ml of tetrahydrofuran was cooled in an ice bath. A 2.34 ml portion of isobutyl chloroformate followed by a 4.13 ml portion of N-methyl morpholine were added. After about 10 minutes, this was poured into a solution of 6-amino-4-chloroquinazoline in 46 ml tetrahydrofuran. This mixture was stirred at room temperature for 2 hours. The mixture was poured into a mixture of brine and saturated sodium bicarbonate and extracted with ether. The ether solution was dried over magnesium sulfate and filtered. The solvent was removed giving [4chloro-6-quinazolinyl]-2-butynamide as colored oil that was used in the next step without additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05760041 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-7e0076e9648b493186c66ae65791e843 |
| Source note | uspto-grants-1998_06 |