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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506256Generated: November 1, 2026

Sodium Hydroxide → HCID 178504209, compound

https://huagongshe.com/reaction/1506256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178504230HCID 178504230—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventDimethylacetamideHCID 31374—
ProductHCID 178504209HCID 17850420973%

Reaction Conditions

Temperature120 °C

Reaction Steps

4-{[trans-4-(Hydroxymethyl)cyclohexyl]amino}-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridine-5-carboxamide (270 mg, 0.645 mmol) in N,N-dimethylacetamide (3 mL) was mixed with N,N-diisopropylethylamine (3 mL) and 1,1′-carbonyldiimidazole (1.04 g, 6.45 mmol) and stirred at 120° C. for 3 hours. The reaction mixture was allowed to cool to room temperature and stirred with 1M aqueous sodium hydroxide (3 mL) and acetonitrile (3 mL) for 5 hours. After addition of water, the reaction mixture was extracted with ethyl acetate, and the organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane=9/1 (v/v)) to give the title compound as a colorless solid (206 mg, yield 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216999B2
Source datasetuspto-grants-2015_12
ORD IDord-b3b36cbe51834e7b812d030831cd448d
Source noteuspto-grants-2015_12