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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19885Generated: October 25, 2026

(4,4-Difluoropiperidin-1-yl)[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]methanone → 6-Bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/19885

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4,4-Difluoropiperidin-1-yl)[5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]methanoneHCID 11603838—
Reactant6-Bromo-5-hydroxy-1H-indole-2-carboxylic acid ethyl esterHCID 67017907—
Product6-Bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indole-2-carboxylic acid ethyl esterHCID 67017929—

Reaction Steps

In analogy to the procedure described for the synthesis of intermediate 1, step 2, the title compound was synthesized from 6-bromo-5-hydroxy-1H-indole-2-carboxylic acid ethyl ester (example 41, step 3). The title compound was obtained in 56% yield as light yellow solid. MS (m/e): 409.0 (MH+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745479B2
Source datasetuspto-grants-2010_06
ORD IDord-0b4f611ff9884dfea65226c4b750e0d2
Source noteuspto-grants-2010_06