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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376917Generated: October 30, 2026

Sodium hydride → N1-methyl-5-(2-amino-5-cyano-4-pyridyl)oxy-1H-1-indolecarboxamide

https://huagongshe.com/reaction/2376917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantCarbamic acid, propyl-, phenyl esterHCID 11252326—
Reactant6-Amino-4-(1H-5-indolyloxy)nicotinonitrileHCID 21949396—
SolventDimethylformamideHCID 6228—
ProductN1-methyl-5-(2-amino-5-cyano-4-pyridyl)oxy-1H-1-indolecarboxamideHCID 2194916422%

Reaction Steps

6-Amino-4-(1H-5-indolyloxy)nicotinonitrile (63 mg, 0.252 mmol) was dissolved in N,N-dimethylformamide (1 ml); and sodium hydride (60% in oil, 11.6 mg, 0.29 mmol) was gradually added thereto while stirring at room temperature. After the reaction mixture was stirred for 30 minutes, phenyl N-propylcarbamate (49.5 mg, 0.277 mmol) was added thereto; and the reaction mixture was stirred for 3 hours. A saturated aqueous solution of ammonium chloride was added thereto; this was subjected to extraction with ethyl acetate, and dried over anhydrous sodium sulfate. This solution was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (Fuji Silysia NH, ethyl acetate-methanol) to yield the title compound (12 mg) and N1-methyl-5-(2-amino-5-cyano-4-pyridyl)oxy-1H-1-indolecarboxamide (17 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468380B2
Source datasetuspto-grants-2008_12
ORD IDord-38df84226070485bba5df3b9f7697357
Source noteuspto-grants-2008_12