HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336923Generated: October 30, 2026
5-Cyano-2-{(4S)-5-cyano-3,6-dimethyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimidin-4-yl}benzenesulfonyl chloride → HCID 66602208, compound
https://huagongshe.com/reaction/336923
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Cyano-2-{(4S)-5-cyano-3,6-dimethyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimidin-4-yl}benzenesulfonyl chloride | HCID 86650721 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66602208 | HCID 66602208 | — |
Reaction Steps
Under argon, 5-cyano-2-{(4S)-5-cyano-3,6-dimethyl-2-oxo-1-[3-(trifluoromethyl)phenyl]-1,2,3,4-tetrahydropyrimidin-4-yl}benzenesulfonyl chloride (52 mg, 105 μmol) was dissolved in dichloromethane (10 ml). Triphenylphosphine-polystyrene resin (capacity 1 mmol/g, 315 mg, 315 μmol, 3 eq.) was added, and the mixture was shaken for 15 h. More triphenylphosphine-polystyrene resin (1 mmol/g, 105 mg, 105 μmol, 1 eq.) was then added, and the mixture was shaken for a further 5 h. The reaction mixture was then filtered, the filtrate was concentrated under reduced pressure and the residue was dried under high vacuum. The title compound was obtained as a solid (90 mg, purity 50%, quant.) which was used without further purification in the subsequent reactions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889700B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-40c61e39590c46e6b9c2c01cd465037c |
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| Source note | uspto-grants-2014_11 |
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