Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 12096337 | HCID 12096337 | — |
| Product | HCID 12093204 | HCID 12093204 | — |
Reaction Steps
Under nitrogen, 2 g of 7-chloro-2-methyl-1-[3-(methylsulfonylamino)propyl]indole are dissolved in 16 ml of TCE at AT and 0.645 ml of oxalyl chloride in 7 ml of TCE is added. The mixture is heated at 120° C. for 16 hours and then cooled to AT. The reaction medium is diluted by adding 20 ml of water and is then poured onto 50 ml of a 10% HCl solution. The mixture is separated by settling out and the aqueous phase is then washed with DCM. The organic phases are combined and then washed with a saturated NaCl solution. Drying over Na2SO4 followed by concentration to dryness are performed and the product is purified by chromatography on silica, elution being carried out with CH2Cl2-MeOH (95/5; v/v). 1.33 g of the expected compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202268B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-302ccc1bc4134d7aa87d4cc8af3fa25c |
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| Source note | uspto-grants-2007_04 |
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