Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715957Generated: October 30, 2026

Methanesulfonyl chloride → methyl 2-(3-methanesulfonyloxypropyl)-5-nitro-1H-indole-4-carboxylate

https://huagongshe.com/reaction/715957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactantmethyl 2-(3-hydroxypropyl)-5-nitro-1H-indole-4-carboxylateHCID 70983888—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Productmethyl 2-(3-methanesulfonyloxypropyl)-5-nitro-1H-indole-4-carboxylateHCID 8671211599.8%

Reaction Steps

Methanesulfonyl chloride (0.176 g) was added to a solution of methyl 2-(3-hydroxypropyl)-5-nitro-1H-indole-4-carboxylate (Intermediate 21, 0.360 g) in pyridine (1 mL) and DCM (10 mL) and the reaction mixture was stirred at room temperature for 4 hours. The mixture was diluted with DCM, washed with aqueous citric acid (5%), aqueous sodium bicarbonate and brine, dried (MgSO4) and filtered. The filtrate was concentrated in vacuo and the residue was dissolved in toluene and evaporated to dryness, four times to give methyl 2-(3-methanesulfonyloxypropyl)-5-nitro-1H-indole-4-carboxylate (0.460 g) as an orange gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187494B2
Source datasetuspto-grants-2015_11
ORD IDord-acc6923098c046a89520401d6a440795
Source noteuspto-grants-2015_11