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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241527Generated: November 3, 2026

Morpholine → (5-bromo-1H-indole-2-yl)(morpholino)methanone

https://huagongshe.com/reaction/2241527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant5-Bromo-1H-indole-2-carboxylic acidHCID 252137—
SolventTetrahydrofuranHCID 8028—
Product(5-bromo-1H-indole-2-yl)(morpholino)methanoneHCID 47154711103.8%

Reaction Steps

A mixture of 5-bromoindole-2-carboxylic acid (5 g, 21 mmol), and 1,1′-carbonyldiimidazole (4.39 g, 27 mmol) in tetrahydrofuran (60 mL) was stirred at room temperature overnight. Morpholine (3.63 mL, 42 mmol) was added and the mixture was stirred for an additional 40 min. The reaction mixture was partitioned between ethyl acetate and an aqueous solution of sodium bicarbonate. The organic layer was washed with hydrochloric acid (1N) and brine, then dried over sodium sulfate, filtered and evaporated in vacuo, to give 6.74 g (99%) of the desired compound as a yellow solid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723325B2
Source datasetuspto-grants-2010_05
ORD IDord-ad63143a01824bed87f43efb349d83db
Source noteuspto-grants-2010_05