HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188643Generated: October 29, 2026
(R)-3-Methylmorpholine → HCID 66993436, compound
https://huagongshe.com/reaction/2188643
Participants
| Role | Name | HCID | Charge |
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| Reactant | (R)-3-Methylmorpholine | HCID 641498 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 8-Benzyl-3-chloro-6,7,8,9-tetrahydropyrazino[2,3-f][1,4]oxazepine | HCID 86648981 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 66993436 | HCID 66993436 | 60% |
Reaction Steps
A suspension of 8-benzyl-3-chloro-6,7,8,9-tetrahydropyrazino[2,3-f][1,4]oxazepine (208 mg), (3R)-3-methylmorpholine (115 mg), Pd2(dba)3 (21 mg), XPhos (44 mg) and sodium tert-butoxide (145 mg) in toluene (5 mL) was stirred under an argon atmosphere with heating at 100° C. for 3 hr. Water was added to the reaction mixture, the aqueous layer was extracted with ethyl acetate, and the organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (solvent gradient: 9→50% ethyl acetate/hexane) to give the title compound (126 mg, 60%) as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324201B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-272cb361428049509929af63a7f8fe96 |
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| Source note | uspto-grants-2012_12 |
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