HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752461Generated: October 28, 2026
Cyanogen Bromide → (R)-4-(6-Bromo-3-fluoro-pyridin-2-yl)-5,5-difluoro-4,6,6-trimethyl-5,6-dihydro-4H-[1,3]oxazin-2-ylamine
https://huagongshe.com/reaction/1752461
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | (R)-2-Methyl-propane-2-sulfinic acid [(R)-1-(6-bromo-3-fluoro-pyridin-2-yl)-2,2,difluoro-3-hydroxy-1,3-dimethyl-butyl]-amide | HCID 86689145 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (R)-4-(6-Bromo-3-fluoro-pyridin-2-yl)-5,5-difluoro-4,6,6-trimethyl-5,6-dihydro-4H-[1,3]oxazin-2-ylamine | HCID 86689146 | 48.9% |
Reaction Steps
A solution of (R)-2-methyl-propane-2-sulfinic acid [(R)-1-(6-bromo-3-fluoro-pyridin-2-yl)-2,2-difluoro-3-hydroxy-1,3-dimethyl-butyl]-amide (2.95 g, 6.84 mmol) and cyanogen bromide (2.24 g, 20.52 mmol) in dry ethanol (68 ml) was sealed with a glass stopper and heated at 85° C. for 9 hr. The reaction solution was evaporated in vacuo and the crude product was taken up with ethyl acetate and 2M aq. ammonia. The organic phase was washed with water and brine, dried over sodium sulfate, filtered and evaporated. The crude product (2.74 g) was chromatographed over silica gel (toluene/ethyl acetate 6:4) to give the title compound as a colourless solid. 1.19 g (48.9% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09163011B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-0297fbcf22fe41e0a60ce95174414990 |
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| Source note | uspto-grants-2015_10 |
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