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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351957Generated: November 3, 2026

(R)-N-[2-benzyloxy-5-(2-iodo-1-triethylsilyloxyethyl)phenyl]methanesulfonamide → HCID 69456203, compound

https://huagongshe.com/reaction/1351957

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-N-[2-benzyloxy-5-(2-iodo-1-triethylsilyloxyethyl)phenyl]methanesulfonamideHCID 54211801—
ReactantHCID 69458689HCID 69458689—
SolventAcetonitrileHCID 6342—
ProductHCID 69456203HCID 6945620337%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of (R)-3-(2-aminopropyl)-1H-indole-6-carboxylic acid diethylamide (20.0 mg, 0.0742 mmol) in acetonitrile (1.0 ml) is added (R)—N-[2-benzyloxy-5-(2-iodo-1-triethylsilyloxyethyl)phenyl]-methanesulfonamide (41.1 mg, 0.0742 mmol), and the mixture is stirred at 110° C. for 21 hours in a sealed vessel. The reaction solution is concentrated under reduced pressure, and the residue is purified by preparative TLC (a saturated ammonia solution in chloroform/methanol=50/1) to give 3-{(2R)-2-[2-(4-benzyloxy-3-methanesulfonylamino-phenyl)-(2R)-2-(triethylsilyloxy) ethylamino]propyl}-1H-indole-6-carboxylic acid diethylamide (19.2 mg, 0.0272 mmol, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217724B2
Source datasetuspto-grants-2007_05
ORD IDord-841068460b044beabb0dbd934bff8288
Source noteuspto-grants-2007_05