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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215496Generated: October 27, 2026

Phenyl Methylcarbamate → HCID 21054849, compound

https://huagongshe.com/reaction/2215496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl MethylcarbamateHCID 16034—
ReactantSodium hydrideHCID 24758—
Reactant5-(6-Amino-pyrimidin-4-yloxy)-1H-indoleHCID 21949266—
SolventDimethylformamideHCID 6228—
ProductHCID 21054849HCID 2105484963.2%

Reaction Steps

Sodium hydride (199 mg, 4.97 mmol) was suspended in N,N-dimethylformamide (10 ml) under nitrogen atmosphere, 6-(1H-indol-5-yloxy)pyrimidin-4-ylamine (1.07 g, 4.73 mmol) synthesized in Production example 2-2 was gradually added while the reaction mixture was stirred at room temperature. After 30 minutes, the reaction mixture was cooled with an ice water bath, then phenyl N-methylcarbamate (751 mg, 4.97 mmol) synthesized in Production example 2-1 was added. The reaction mixture was heated to room temperature and stirred for 1 hour. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with water and brine, and was dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by silica gel column chromatography (eluent; ethyl acetate) to yield the title compound (847 mg, 2.99 mmol, 63%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109219B2
Source datasetuspto-grants-2006_09
ORD IDord-d40e5e92863a4e88abca819a5d607300
Source noteuspto-grants-2006_09