Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 6-Methyl-4'-trifluoromethylbiphenyl-2-carboxylic acid chloride | HCID 11055639 | — |
| Reactant | (R)-Methyl (5-amino-2,3-dihydro-1H-inden-2-yl)carbamate | HCID 11413084 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Dimethyl Sulfide | HCID 1068 | — |
| Product | (r)-6-Methyl-4'-trifluoromethylbiphenyl-2-carboxylic acid (2-methoxycarbonylaminoindan-5-yl)-amide | HCID 9869236 | — |
Reaction Steps
To an ice bath cooled solution of (R)-(5-aminoindan-2-yl)-carbamic acid methyl ester (9.5 g, 46.1 mmol), ([α]D=−26.29° (c=9.87 mg/mL, DMSO); mp 144-145° C.) and pyridine (4.48 mL, 55.5 mmol) in 200 mL of methylene chloride is added 6-methyl-4′-trifluoromethylbiphenyl-2-carboxylic acid chloride ( 80.5 mL of a 0.63 M solution in methylene chloride, 50.7 mmol). The reaction is stirred for 15 minutes at room temperature. The mixture is washed with 1N HCl, bicarbonate and brine. The organic layer is dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The product is purified by crystallization from ethyl acetate/hexanes (1:2) to give (R)-6-methyl-4′-trifluoromethylbiphenyl-2-carboxylic acid (2-methoxycarbonylaminoindan-5-yl)-amide as a crystalline solid, mp 112-114° C. [α]D=−12.85°, c=11.36 mg/mL DMS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06197798B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-993606a201e84e4a9ceb930785f13034 |
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| Source note | uspto-grants-2001_03 |
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