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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958644Generated: October 31, 2026

N-bromobutanimide → HCID 59508087, compound

https://huagongshe.com/reaction/1958644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 59508063HCID 59508063—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59508087HCID 59508087—

Reaction Conditions

Temperature60 °C

Reaction Steps

A suspension of 2-(2-methoxypyridin-3-yl)-N-(3-morpholinopropyl)-1H-indole-5-carboxamide (0.850 g, 0.215 mmol) in 100 ml THF was heated to 60° C. until dissolved. To the solution was added N-bromosuccinimide (0.406 g, 0.263 mmol) and the reaction was allowed to stir for 1.5 hours. The reaction was not complete, so more N-bromosuccinimide (0.062 g, 0.35 mmol; 0.040 g, 0.022 mmol) was added sequentially and the reaction stirred for 10 more minutes after each addition. Upon completion, the reaction was concentrated and to the residue was added 50 ml EtOAC and 100 ml water. The organics were separated, washed with water (50 ml) and brine (25 ml) and concentrated. The crude product was used with no further purification. LCMS: 473 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410144B2
Source datasetuspto-grants-2013_04
ORD IDord-91889ed1093745c5b71c9786d3576afa
Source noteuspto-grants-2013_04