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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724323Generated: October 30, 2026

Isobutyric Acid → HCID 178503217, compound

https://huagongshe.com/reaction/724323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyric AcidHCID 6590—
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 178503208HCID 178503208—
SolventDimethylformamideHCID 6228—
ProductHCID 178503217HCID 178503217101.6%

Reaction Steps

N-(cis-4-Amino-cyclohexyl)-5-fluoro-2-(3-methylsulfanyl-phenoxy)-nicotinamide hydrochloride (100 mg, 0.243 mmol) was dissolved in dimethylformamide (1 ml) and triethylamine (100 μl, 0.729 mmol) was added followed by isobutyric acid (27 μl, 0.291 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (56 mg, 0.291 mmol) and 1-hydroxybenzotriazole (39 mg, 0.291 mmol). The reaction was stirred under nitrogen at room temperature for 64 h and the solvent was removed under reduced pressure. The residue was partitioned between sat. sodium bicarbonate solution (5 ml) and ethyl acetate (10 ml) and the aqueous phase was extracted with ethyl acetate (3×10 ml). The combined organic extracts were washed with water (2×5 ml), brine (5 ml), dried over MgSO4 and the solvent was removed under reduced pressure. The residue was triturated with diethylether (5 ml) to give 5-Fluoro-N-(cis-4-isobutyrylamino-cyclohexyl)-2-(3-methylsulfanyl-phenoxy)-nicotinamide (110 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141586B2
Source datasetuspto-grants-2006_11
ORD IDord-1e257e2966e446e8af9a939b44b2b5fa
Source noteuspto-grants-2006_11