HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355244Generated: October 31, 2026
Dimethyl Sulfone → 1-[1-(3-amino-3-methyl-butyl)-1H-indol-5-yl]-2-methanesulphonyl-ethanone
https://huagongshe.com/reaction/2355244
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfone | HCID 6213 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Methyl 1-(3-amino-3-methyl-butyl)-indole-5-carboxylate | HCID 68453514 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-[1-(3-amino-3-methyl-butyl)-1H-indol-5-yl]-2-methanesulphonyl-ethanone | HCID 58875119 | — |
Reaction Steps
Potassium tert. butoxide (741 mg, 6.62 mmol) is added in two batches to a solution of dimethylsulphone (661 mg, 7.03 mmol) in 5 ml DMSO. After 10 minutes stirring at RT a solution of methyl 1-(3-amino-3-methyl-butyl)-indole-5-carboxylate (Component IV) (520 mg, 2.00 mmol) in 2 ml DMSO is added dropwise over 10 minutes. The reaction mixture is stirred for 16 hours at 70° C., acidified with TFA while cooling with ice and chromatographed on Microsorb C18-reverse-phase [acetonitrile (0.1% TFA)/water (0.13% TFA)=10:90→100:0]. Then the residue is chromatographed again on silica gel (DCM/methanol/ammonia=90:9:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07754756B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-ac0047c543f243908115cd041dabe2dc |
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| Source note | uspto-grants-2010_07 |
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