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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404153Generated: November 1, 2026

4-(benzyloxy)-7-bromo-5-fluoro-1-methyl-1H-indole → 6-bromo-7-propyl-3,7-dihydro-2H-[1,4]dioxino[2,3-e]indole

https://huagongshe.com/reaction/1404153

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(benzyloxy)-7-bromo-5-fluoro-1-methyl-1H-indoleHCID 58303958—
Reactant6-bromo-3,7-dihydro-2H-[1,4]dioxino[2,3-e]indoleHCID 66927131—
Product6-bromo-7-propyl-3,7-dihydro-2H-[1,4]dioxino[2,3-e]indoleHCID 6692721990%

Reaction Steps

Following the procedure (step 2, scheme 33) used to prepare compound 33-3, compound 40-2 gave compound 40-3 in 90% yield as a yellow solid. LCMS: calc 295.0 found 296.0 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912220B2
Source datasetuspto-grants-2014_12
ORD IDord-2768aac443b44f7bbf9278d51641dd9e
Source noteuspto-grants-2014_12