Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904456Generated: October 27, 2026

Methyl phenyl sulfone → 6-(2-Ethylhexanamido)-1-[2-methoxy-4-[2-(phenylsulphonyl)acetyl]benzyl]indole

https://huagongshe.com/reaction/1904456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl phenyl sulfoneHCID 18369—
ReactantMonobasic potassium phosphateHCID 516951—
Reactant4-[6-(2-ethylhexanamido)indole-1-yl-methyl]-3-methoxybenzoic N,N-diphenylcarbamic anhydrideHCID 14753011—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product6-(2-Ethylhexanamido)-1-[2-methoxy-4-[2-(phenylsulphonyl)acetyl]benzyl]indoleHCID 1475307044.1%

Reaction Steps

A solution of butyllithium (0.86 ml of a 2.3M solution in hexanes) was added to a solution of methyl phenyl sulphone (312 mg) in dry tetrahydrofuran (THF) (5 ml.) at -78° C. After 15 minutes a white suspension formed. To this mixture was then added a solution of 4-[6-(2-ethylhexanamido)indole-1-yl-methyl]-3-methoxybenzoic N,N-diphenylcarbamic anhydride (A) (500 mg) in THF (4 ml). After two hours, the mixture was allowed to warm to ambient temperature and an excess of a saturated solution of potassium dihydrogen phosphate was added. The solvent was removed by evaporation and the residue was partitioned between water and ethyl acetate. The organic phase was dried (Na2SO4) and evaporated. The residual gum was purified by chromatography on silica gel (20 g), using 2:98 v/v ether:methylene chloride as eluent, to give the title compound as a white solid (200 mg, 44%); mp 131°-133° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837235
Source datasetuspto-grants-1989_06
ORD IDord-298b5c9017c04d1ea6b479ebe7d08515
Source noteuspto-grants-1989_06