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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502131Generated: October 31, 2026

Dichloromethane → HCID 59426369, compound

https://huagongshe.com/reaction/502131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAmmonium HydroxideHCID 14923—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 59425724HCID 59425724—
SolventDimethylformamideHCID 6228—
ProductHCID 59426369HCID 5942636985%

Reaction Steps

1-Ethyl-1H-indole-3,6-dicarboxylic acid 6-methyl ester (600 mg, 2.43 mmol) is suspended in a solution of CH2Cl2 (27 ml) and DMF (20 μL). Oxalyl chloride (470 μL, 5.38 mmol) is added, and the reaction mixture is stirred for 1 hour at room temperature. This mixture is then slowly poured into a rapidly stirring solution of concentrated NH4OH (10 mL). This is then partitioned in H2O and EtOAc. The residue from the ethyl acetate layer is triturated with acetone to yield 6-methoxycarbonyl-1-ethyl-1H-indole-3-carboxamide (511 mg, 85%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772271B2
Source datasetuspto-grants-2010_08
ORD IDord-7dcd740308f84879b7564249d5e3f575
Source noteuspto-grants-2010_08