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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492807Generated: October 27, 2026

Phenylacetyl isocyanate → Morpholine-4-carboxylic acid {4-[2-fluoro-4-(3-phenylacetylureido)phenoxy]pyridin-2-yl}amide

https://huagongshe.com/reaction/492807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl isocyanateHCID 12259960—
ReactantN-(4-(4-amino-2-fluorophenoxy)pyridin-2-yl)morpholine-4-carboxamideHCID 57677752—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
SolventPyrrolidine-1-carboxylic acid {6-[2-fluoro-4-(3-phenylacetylthioureido)phenoxy]pyrimidin-4-yl}amideHCID 11248939—
ProductMorpholine-4-carboxylic acid {4-[2-fluoro-4-(3-phenylacetylureido)phenoxy]pyridin-2-yl}amideHCID 5767750012%

Reaction Steps

To a solution of morpholine-4-carboxylic acid [4-(4-amino-2-fluorophenoxy)pyridin-2-yl]amide (54 mg) in N,N-dimethylformamide (1.0 ml) was added a solution of phenylacetyl isocyanate in hexane (0.972 ml, Production Example 1), followed by stirring at room temperature for 25 hrs. The reaction mixture was partitioned between ethyl acetate (50 ml) and water (30 ml). The organic layer was washed with brine, and dried over anhydrous sodium sulfate. The solvent was evaporated to give a residue, which was then purified by silica gel column chromatography (eluent; hexane:ethyl acetate=1:1 to 1:2, ethyl acetate, ethyl acetate:methanol=20:1 to 10:1). Fractions containing the target compound were concentrated to give a solid, which was suspended in ethyl acetate. The solid was filtered off, washed with ethyl acetate, and dried under aeration to provide the titled compound (9.5 mg, 12%) as colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531532B2
Source datasetuspto-grants-2009_05
ORD IDord-df66b798e50740588604c3b2122cdee4
Source noteuspto-grants-2009_05