HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276831Generated: October 26, 2026
4-Methylmorpholine → HCID 15550657, compound
https://huagongshe.com/reaction/276831
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | 6-Amino-4-(3-bromo-phenylamino)-[1,8]naphthyridine-3-carbonitrile | HCID 9949813 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15550657 | HCID 15550657 | 17.9% |
Reaction Steps
To a solution of 1.4 g (4.12 mmol) of 6-amino-4-(3-bromo-phenylamino)-[1.8]naphthyridine-3-carbonitrile and 1.67 g (16.5 mmol) of N-methyl-morpholine in a mixture of 6 ml of N,N-dimethylformamide and 35 ml of tetrahydrofuran was added with stirring at 0° C. a solution of 0.52 g (5.76 mmol) of acryloyl chloride in 10 ml of tetrahydrofuran over 10 min. After 3 hr at 0° C., the most of the solvent was removed saturated sodium bicarbonate was added. Solid was collected and washed with water. After air drying, the solid was extracted with 500 ml of boiling tetrahydrofuran. The tetrahydrofuran was removed and the residue was purified on a silica gel column eluting with ethyl acetate-methanol mixtures giving 0.29 g of the title compound as a yellow solid: mass spectrum (electrospray, m/e): M+H 394, 396.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06355636B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-5abdc1b6973648d9bbaa66457a36d986 |
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| Source note | uspto-grants-2002_03 |
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