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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651705Generated: October 31, 2026

Potassium → (R)-N-Benzyloxymethyl-1-[1-benzyloxymethyl-3-(1-methyl-2-pyrrolidinylmethyl)-1H-indol-5-yl]-N-methylmethanesulfonamide

https://huagongshe.com/reaction/651705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassiumHCID 5462222—
Reactantn-Benzyloxymethyl-1-[(r)-1-benzyloxymethyl-3-(1-methyl-2-pyrrolidinylmethyl)-1h-indol-5-yl]-1-cyano-n-methylmethanesulfonamideHCID 54237060—
Product(R)-N-Benzyloxymethyl-1-[1-benzyloxymethyl-3-(1-methyl-2-pyrrolidinylmethyl)-1H-indol-5-yl]-N-methylmethanesulfonamideHCID 5368333333%

Reaction Steps

To a stirred solution of N-benzyloxymethyl-1-[(R)-1-benzyloxymethyl-3-(1-methyl-2-pyrrolidinylmethyl)-1H-indol-5-yl]-1-cyano-N-methylmethanesulfonamide (from step (e), 2.0 g, 3.4 mmol) in IMS (14 ml) at ambient temperature was added 2N potassium hydrodroxide solution (7 ml, 14 mmol). The dark brown solution was then brought to reflux and maintained at this temperature for 15 hr. The oily reaction mixture was then cooled to ambient temperature and extracted with ethyl acetate (3×20 ml). The organic extracts were combined and evaporated in vacuo to yield a dark brown oil. This was purified by flash column chromatography (ethyl acetate:triethylamine 95:5 as eluant) to yield the subtitle compound (631 mg, 33%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281357B1
Source datasetuspto-grants-2001_08
ORD IDord-f8c420b3e7b842bab2203d56864b299e
Source noteuspto-grants-2001_08