HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068995Generated: October 31, 2026
4-Methylmorpholine → HCID 131722712, compound
https://huagongshe.com/reaction/1068995
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N4-(3-Bromophenyl)quinazoline-4,6-diamine | HCID 5328042 | — |
| Reactant | HCID 21190749 | HCID 21190749 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 131722712 | HCID 131722712 | — |
Reaction Steps
Isobutyl chloroformate (0.845 g, 6.2 mmol) and N-methylmorpholine (1.0 g, 9.9 mmol) were added to an ice cold solution of 1.8 g (9.67 mmol) of diisopropyl-amino-but-2-ynoic acid in 100 mL of tetrahydrofuran under nitrogen. After stirring for 30 min, a solution of 1.500 g of N-(3-bromophenyl)-4,6-quinazolindiamine in 15 mL of pyridine was added and the mixture was stirred for 2 hr at 0° C. The reaction was then quenched with ice water, poured into saturated sodium bicarbonate, and the product was extracted with ethyl acetate. Chromatography of the extract on silica gel, eluting with methanol/ethyl acetate (5:95), gave 1.54 g of diisopropyl-methyl-amino-but-2-ynoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amide: mass spectrum (m/e): M+H 480.
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-627ca5b6a25045adbbad27fda2167f48 |
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| Source note | uspto-grants-2001_06 |
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