Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | 3-(4-Methoxyphenyl)-4-methylisothiazol-5-amine | HCID 53401080 | — |
| Reactant | HCID 67180743 | HCID 67180743 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Mglu1 C-11 | HCID 57404255 | 80.4% |
Reaction Steps
Add trimethylaluminum (2 M in toluene, 3.59 g, 45.5 mmol) to a 0° C. solution of 3-(4-methoxyphenyl)-4-methylisothiazol-5-ylamine (10.0 g, 45.5 mmol) in dichloromethane (455 mL). Stir 5 min and add benzyl (R,R)-2-methylcyclopropane-carboxylate (8.64 g, 45.5 mmol). Heat to 50° C. with nitrogen flow to remove solvent. The resulting oil is heated at 50° C. for 3 h. Quench with water and dilute with EtOAc (300 mL). Wash with 0.1 N HCl, dry (K2CO3), evaporate, and crystallize from hexane/EtOAc to afford (R,R)—N-[3-(4-methoxyphenyl)-4-methylisothiazol-5-yl]-2-methylcyclopropanecarboxamide. Yield: 80.4%. ES-MS: m/e 303.0 (m+1). (The mother liquor may be used for further recrystallizations.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960419B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-b40c04fcb93d479c82f7717750b0d3ad |
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| Source note | uspto-grants-2011_06 |
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