HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → methyl 2-(3-methanesulfonyloxypropyl)-5-nitro-1H-indole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | methyl 2-(3-hydroxypropyl)-5-nitro-1H-indole-4-carboxylate | HCID 70983888 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | methyl 2-(3-methanesulfonyloxypropyl)-5-nitro-1H-indole-4-carboxylate | HCID 86712115 | 99.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187494B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-acc6923098c046a89520401d6a440795 |
| Source note | uspto-grants-2015_11 |