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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl phenyl sulfone | HCID 18369 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | 4-[6-(2-ethylhexanamido)indole-1-yl-methyl]-3-methoxybenzoic N,N-diphenylcarbamic anhydride | HCID 14753011 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(2-Ethylhexanamido)-1-[2-methoxy-4-[2-(phenylsulphonyl)acetyl]benzyl]indole | HCID 14753070 | 44.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04837235 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-298b5c9017c04d1ea6b479ebe7d08515 |
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| Source note | uspto-grants-1989_06 |
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