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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376869Generated: October 30, 2026

Water → 5-[(2-Amino-4-pyridinyl)oxy]-N-cyclopentyl-1H-indole-1-carboxamide

https://huagongshe.com/reaction/2376869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantPhenyl cyclopentylcarbamateHCID 12791466—
Reactant4-(1H-5-indolyloxy)-2-pyridinamineHCID 21949365—
SolventDimethylformamideHCID 6228—
Product5-[(2-Amino-4-pyridinyl)oxy]-N-cyclopentyl-1H-indole-1-carboxamideHCID 2194912255.7%

Reaction Steps

4-(1H-5-Indolyloxy)-2-pyridinamine (2.50 g, 11.1 mmol, CAS No. 417722-11-3), which was described in WO 02/32872, was dissolved in N,N-dimethylformamide (30 ml); sodium hydride (0.530 g, 13.3 mmol) was added thereto at room temperature; and the reaction mixture was stirred for 30 minutes. Phenyl N-cyclopentylcarbamate (2.50 g, 12.2 mmol) was added thereto at room temperature while stirring; and the reaction mixture was stirred for 30 minutes. Water was added to the reaction mixture; and the precipitated crystals were filtered off, and washed with water. This crystals were dissolved in methanol, and purified by silica gel column chromatography (Fuji Silysia NH; hexane:ethyl acetate=1:1, ethyl acetate, ethyl acetate:methanol=98:2 in this order). The obtained crystals were suspended in hexane: ethanol=10:1, filtered off, washed with hexane, and dried under aeration to yield the title compound as colorless crystals (2.08 g, 6.18 mmol, 55.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468380B2
Source datasetuspto-grants-2008_12
ORD IDord-632fa6e5c4a44f77995c572bf4f62275
Source noteuspto-grants-2008_12