Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227500Generated: October 30, 2026

ethyl 5-iodo-3-{[2-(phenoxymethyl)morpholin-4-yl]sulfonyl}-1-(phenylsulfonyl)-1H-indole-2-carboxylate → (R)-5-Iodo-3-{[2-(phenoxymethyl)morpholin-yl]sulfonyl}-1H-indole-2-carboxamide

https://huagongshe.com/reaction/227500

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 5-iodo-3-{[2-(phenoxymethyl)morpholin-4-yl]sulfonyl}-1-(phenylsulfonyl)-1H-indole-2-carboxylateHCID 68442554—
ReactantEthyl (+/-)-5-chloro-3-{[2-(phenoxymethyl)morpholin-4-yl]sulfonyl}-1-(phenylsulfonyl)-1h-indole-2-carboxylateHCID 68878207—
Product(R)-5-Iodo-3-{[2-(phenoxymethyl)morpholin-yl]sulfonyl}-1H-indole-2-carboxamideHCID 57756163—

Reaction Steps

Using the same procedures described for Example 23, replacing the product from Step A of Example 22, ethyl(±)-5-chloro-3-{[2-(phenoxymethyl)morpholin-4-yl]sulfonyl}-1-(phenylsulfonyl)-1H-indole-2-carboxylate, with ethyl(±)-5-iodo-3-{[2-(phenoxymethyl)morpholin-1-yl]sulfonyl}-1-(phenylsulfonyl)-1H-indole-2-carboxylate, the second-eluting enantiomer of ethyl 5-iodo-3-{[2-(phenoxymethyl)morpholin-4-yl]sulfonyl}-1-(phenylsulfonyl)-1H-indole-2-carboxylate was converted to the titled compound after purification by preparative reversed phase HPLC. Proton NMR for the product was consistent with the titled compound. ESI+MS: 542.82 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560546B2
Source datasetuspto-grants-2009_07
ORD IDord-70f2af851f3d4efb81ab733f4edb8d26
Source noteuspto-grants-2009_07