HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921065Generated: October 29, 2026
Tri-o-tolylphosphine → (E)-N-methyl-N-(1-methyl-1H-indol-2-ylmethyl)-3-(2-oxo-1,4-dihydro-2H-pyrido[2,3-d]-1,3-oxazin-6yl)acrylamide
https://huagongshe.com/reaction/1921065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-bromo-1H,2H,4H-pyrido(2,3-d)(1,3)oxazin-2-one | HCID 15925990 | — |
| Reactant | N-Methyl-N-[(1-methyl-2-indolyl)methyl]acrylamide | HCID 20752825 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Propionitrile | HCID 7854 | — |
| Product | (E)-N-methyl-N-(1-methyl-1H-indol-2-ylmethyl)-3-(2-oxo-1,4-dihydro-2H-pyrido[2,3-d]-1,3-oxazin-6yl)acrylamide | HCID 9821027 | 55.3% |
Reaction Steps
To a stirred solution of N-methyl-N-(1-methyl-1H-indol-2-ylmethyl)acrylamide (1.19 g, 5.2 mmole) in propionitrile (50 mL) was added 6-bromo-2-oxo-1,4-dihydro-2H-pyrido[2,3-d]-1,3-oxazine (1.1 g, 4.9 mmole), DIEA (1.75 mL, 10 mmole), palladium(II) acetate (112 mg, 0.5 mmole), and tri-o-tolylphosphine (304 mg, 1.0 mmole). The reaction was purged with argon and heated at reflux for 16 hr, then was cooled to RT and concentrated under vacuum. The residue was taken up in CHCl3 and the solution was filtered through a pad of silica gel (3% methanol/CHCl3). The filtrate was concentrated and the residue was triturated with ethyl acetate, collected by suction filtration, and dried under vacuum gave the title compound (1.02 g, 55%) as an off-white solid: LCMS (ES) m/e 377 4 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173646B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-1b985aaefdb54dfb9e07d7e422b1a7cf |
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| Source note | uspto-grants-2012_05 |
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