HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245359Generated: October 26, 2026
Barbituric Acid → (2r,4s,4As)-8-acetyl-9,10-difluoro-2,4-dimethyl-1,2,4,4a-tetrahydro-2'h,6h-spiro[1,4-oxazino[4,3-a]quinoline-5,5'-pyrimidine]-2',4',6'(1'h,3'h)-trione
https://huagongshe.com/reaction/245359
Participants
| Role | Name | HCID | Charge |
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| Reactant | Barbituric Acid | HCID 6211 | — |
| Reactant | 5-acetyl-2-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzaldehyde | HCID 58847058 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | (2r,4s,4As)-8-acetyl-9,10-difluoro-2,4-dimethyl-1,2,4,4a-tetrahydro-2'h,6h-spiro[1,4-oxazino[4,3-a]quinoline-5,5'-pyrimidine]-2',4',6'(1'h,3'h)-trione | HCID 58847042 | — |
Reaction Steps
To a solution of 5-acetyl-2-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzaldehyde (Intermediate 11, 3.0 g, 9.17 mmol) in IPA was added barbituric acid (1.4 g, 11.00 mmol), and the mixture was heated at 85° C. for 12 hours. Solvents were evaporated and the residue was purified over neutral alumina using a gradient of methanol in CH2Cl2 to give the title compound as a racemic mixture in the form of an off-white solid. Yield: 3.0 g (75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658641B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-3a2ef7a8c82541e096659b691eb6fea3 |
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| Source note | uspto-grants-2014_02 |
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