HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536955Generated: October 31, 2026
Trifluoroacetic acid → HCID 71157223, compound
https://huagongshe.com/reaction/536955
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium methanesulfinate | HCID 2733271 | — |
| Reactant | HCID 24874733 | HCID 24874733 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 71157223 | HCID 71157223 | 21% |
Reaction Steps
To a mixture of 5-cyano-1H-imidazole-2-carboxylic acid [2-cyclohex-1-enyl-4-(4-hydroxy-tetrahydro-pyran-4-yl)-phenyl]-amide (as prepared in Example 27, 75 mg, 0.19 mmol) and sodium methylsulfinate (195 mg, 1.90 mmol) in 4 mL of methanol was added 0.28 mL (3.80 mmol) of TFA. The mixture was stirred overnight at 70° C. and then concentrated in vacuo. The crude residue was partitioned in EtOAc (20 mL) and saturated aqueous NaHCO3 (20 mL). The organic layer was dried (Na2SO4) and then concentrated in vacuo. The residue was purified by preparative TLC on silica gel (20% ethyl acetate-hexane) to afford the title compound as a light brown oil (18 mg, 21%). 1H-NMR (CDCl3; 400 MHz): δ 9.64 (s, 1H), 8.32 (d, 1H, J=8.0), 7.71 (s, 1H), 7.33 (m, 1H), 7.23 (d, 1H, J=1.8 Hz), 5.87 (s, 1H), 3.90-3.81 (m, 4H), 3.01 (s, 3H), 2.30-2.25 (m, 4H), 2.07-1.79 (m, 8H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859602B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-3bacc02155ca4ee7a43e57111ac13930 |
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| Source note | uspto-grants-2014_10 |
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