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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493993Generated: November 1, 2026

[6-Bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(1,1-Dioxo-1lambda6-thiomorpholin-4-yl)-methanone → [6-Bromo-1-isopropyl-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(1,1-dioxo-1lambda6-thiomorpholin-4-yl)-methanone

https://huagongshe.com/reaction/493993

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[6-Bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(1,1-Dioxo-1lambda6-thiomorpholin-4-yl)-methanoneHCID 16739609—
ReactantIsopropyl-methanesulfonateHCID 22141912—
Product[6-Bromo-1-isopropyl-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(1,1-dioxo-1lambda6-thiomorpholin-4-yl)-methanoneHCID 16739675—

Reaction Steps

In analogy to the procedure described for the synthesis of example 3, the title compound was synthesized from [6-bromo-5-(1-isopropyl-piperidin-4-yloxy)-1H-indol-2-yl]-(1,1-dioxo-1λ6-thiomorpholin-4-yl)-methanone (Example 6, step 4) and isopropylmethanesulfonate. The desired product was obtained in a yield of 69% as light yellow solid. MS (m/e): 540.3 (M+H, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538101B2
Source datasetuspto-grants-2009_05
ORD IDord-6bf0ea85da1c4483a0f57755b6be77fd
Source noteuspto-grants-2009_05