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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445208Generated: November 1, 2026

Methanol → HCID 178511103, compound

https://huagongshe.com/reaction/1445208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAcrylonitrileHCID 7855—
ReactantTriethylamineHCID 8471—
Reactant4-Cyano-1h-imidazole-2-carboxylic acid (2-cyclohex-1-enyl-4-piperidin-4-yl-phenyl)-amide trifluoroacetic acid saltHCID 178510383—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 178511103HCID 17851110395.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A flask was charged with 4-cyano-1H-imidazole-2-carboxylic acid (2-cyclohex-1-enyl-4-piperidin-4-yl-phenyl)-amide TFA salt (77 mg, 0.16 mmol) (as prepared in Example 14, step (b)), NEt3 (24 μL, 0.16 mmol), acrylonitrile (12 μL, 0.18 mmol), 0.1 mL MeOH and 1.0 mL of 1,2-dichloroethane and stirred for 1 h at 80° C. The reaction was concentrated and the title compound was purified by RP-HPLC (C18), eluting with 30-50% CH3CN in 0.1% TFA/H2O over 12 min to give 83 mg (95%) of a white solid. 1H-NMR (400 MHz, CD3OD): δ 8.18 (d, 1H), 8.06 (m, 1H), 7.22 (dd, 1H), 7.12 (d, 1H), 5.82 (m, 1H), 3.76 (m, 2H), 3.60 (m, 2H), 3.28 (t, 2H), 3.12 (t, 2H), 2.92 (m, 1H), 2.30 (m, 4H), 2.18-1.98 (m, 4H), 1.92-1.74 (m, 4H). Mass spectrum (ESI, m/z): Calcd. for C25H28N6O, 429.2 (M+H), found 429.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662837B2
Source datasetuspto-grants-2010_02
ORD IDord-c03904aeaf8544569aa37c0b450e4d71
Source noteuspto-grants-2010_02