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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502135Generated: October 30, 2026

Dichloromethane → HCID 59426170, compound

https://huagongshe.com/reaction/502135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAmmonium HydroxideHCID 14923—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 53415958HCID 53415958—
SolventDimethylformamideHCID 6228—
ProductHCID 59426170HCID 5942617054%

Reaction Steps

1-Ethyl-6-methoxy-1H-indole-3-carboxylic acid (250 mg, 1.14 mmol) is suspended in a solution of CH2Cl2 (12.5 mL) and DMF (10 μL). Oxalyl chloride (230 μL, 2.64 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 (5 mL). This is then partitioned in H2O and EtOAc. The residue from the ethyl acetate layer is triturated with acetone to yield 1-ethyl-6-methoxy-1H-indole-3-carboxamide (134 mg, 54%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772271B2
Source datasetuspto-grants-2010_08
ORD IDord-3c6f97dfbf214d48820a0cb2e5585cf8
Source noteuspto-grants-2010_08