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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054274Generated: November 2, 2026

Trifluoroacetic acid → HCID 71157223, compound

https://huagongshe.com/reaction/1054274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium methanesulfinateHCID 2733271—
ReactantHCID 24874733HCID 24874733—
SolventMethanolHCID 887—
ProductHCID 71157223HCID 7115722321%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394289B2
Source datasetuspto-grants-2016_07
ORD IDord-ef9e6a4ce6fd45b58440f15b44faf12f
Source noteuspto-grants-2016_07