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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372631Generated: November 1, 2026

Pyridine → Ethyl 3-chloro-4-(1-indolinylcarbonylamino)phenylacetate

https://huagongshe.com/reaction/1372631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantIndolineHCID 10328—
ReactantTriphosgeneHCID 94429—
Reactant(4-Amino-3-chloro-phenyl)-acetic acid ethyl esterHCID 17859298—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-chloro-4-(1-indolinylcarbonylamino)phenylacetateHCID 17859294274.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

In methylene chloride (50 ml), triphosgene (926 mg, 3.12 mmol) and then pyridine (5 ml) were added to ethyl 4-amino-3-chlorophenylacetate (2.00 g, 9.36 mmol) under stirring at 0° C. After stirring at the same temperature for 15 minutes, indoline (1.05 ml, 9.36 mmol) was added. The reaction mixture was further stirred for 15 minutes at room temperature. Water (50 ml) was added to the reaction mixture, followed by extraction with ethyl acetate (300 ml). The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and distilled under reduced pressure to remove the solvent, whereby ethyl 3-chloro-4-(1-indolinylcarbonylamino)phenylacetate (3.07 g, 91%) was obtained as a pale pink crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-c43f230416f64fb091f51102625deac3
Source noteuspto-grants-2007_01