HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068990Generated: November 2, 2026
4-Methylmorpholine → HCID 86757051, compound
https://huagongshe.com/reaction/1068990
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N4-(3-Bromophenyl)quinazoline-4,6-diamine | HCID 5328042 | — |
| Reactant | HCID 21190740 | HCID 21190740 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86757051 | HCID 86757051 | 25.1% |
Reaction Steps
Isobutyl chloroformate (0.845 g, 6.2 mmol) and N-methylmorpholine (1.2 g, 11.9 mmol) were added to an ice cold solution of 1.6 g (9.52 mmol) of (2-methoxy-ethyl)-methyl-amino-but-2-ynoic acid in 50 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, then it was 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 (15:85), gave 0.560 g of (2-methoxy-ethyl)-methyl-amino-but-2-ynoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amide: mass spectrum (m/e): M+H 468.
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-d052709e40dd476cb1ddb0b82d32881b |
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| Source note | uspto-grants-2001_06 |
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