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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404154Generated: October 31, 2026

2-(4-(benzyloxy)-7-bromo-5-fluoro-1-methyl-1H-indol-3-yl)acetic acid → 2-(6-bromo-7-propyl-3,7-dihydro-2H-[1,4]dioxino[2,3-e]indol-9-yl)acetic acid

https://huagongshe.com/reaction/1404154

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-(benzyloxy)-7-bromo-5-fluoro-1-methyl-1H-indol-3-yl)acetic acidHCID 58304036—
Reactant6-bromo-7-propyl-3,7-dihydro-2H-[1,4]dioxino[2,3-e]indoleHCID 66927219—
Product2-(6-bromo-7-propyl-3,7-dihydro-2H-[1,4]dioxino[2,3-e]indol-9-yl)acetic acidHCID 6692732174%

Reaction Steps

Following the procedure (step 3, scheme 333) used to prepare compound 33-4, compound 40-3 gave compound 40-4 in 74% yield as a yellow solid. LCMS: calc 353.0 found 353.9 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912220B2
Source datasetuspto-grants-2014_12
ORD IDord-3286cd95e0a848d9a8a3e2ce719621ac
Source noteuspto-grants-2014_12