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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387247Generated: October 25, 2026

1,2-Dichloroethane → 5-bromo-1H-indole-7-carboxamide

https://huagongshe.com/reaction/387247

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAmmoniaHCID 222—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant5-Bromo-1H-indole-7-carboxylic acidHCID 53399257—
SolventDichloromethaneHCID 6344—
Product5-bromo-1H-indole-7-carboxamideHCID 5960065799.6%

Reaction Steps

To a solution of 5-bromo-1H-indole-7-carboxylic acid (10.0 g, 42 mmol) in CH2Cl2 (100 mL) at room temperature, EDC (9.66 g, 50.4 mmol), HOBt (6.81 g, 50.4 mmol) and NH3 (2.0 M in MeOH, 84 mL, 168 mmol) were added. The reaction mixture was stirred at room temperature for 16 hours. The solvent was evaporated and the residue partitioned between ethyl acetate (100 mL) and water (100 mL). The water layer was extracted with ethyl acetate (2×100 mL) and the combined organic phase was dried over MgSO4 and concentrated to give 10 g (98%) of the title compound as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372875B2
Source datasetuspto-grants-2013_02
ORD IDord-4b8e6359d2104118a29f2f769e26d6cd
Source noteuspto-grants-2013_02