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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009523Generated: October 31, 2026

Aniline → HCID 11680840, compound

https://huagongshe.com/reaction/1009523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantDichloromethane ethylacetateHCID 21226138—
ReactantHCID 59424944HCID 59424944—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11680840HCID 1168084051%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 3-cyano-1-ethyl-1H-indole-6-carbonyl chloride (70 mg, 0.30 mmol) in THF (5 mL) is cooled to 0° C. and treated with aniline (0.08 mL, 0.90 mmol). After the addition, the reaction is warmed to ambient temperature and after stirring for an additional 16 hours, the reaction mixture is diluted with H2O and extracted with EtOAc (2×). The combined organic phases are washed with saturated NaCl and then dried and concentrated to afford the product. Chromatography (EtOAc/CH2Cl2, 2/98) over silica gel gives 44 mg (51%) of 3-cyano-1-ethyl-1H-indole-6-carboxylic acid phenylamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973069B2
Source datasetuspto-grants-2011_07
ORD IDord-cbe69d1aaa614dbd9ddaefdb689a2bbf
Source noteuspto-grants-2011_07