Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 23110289 | HCID 23110289 | — |
| Reactant | HCID 59694308 | HCID 59694308 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23110281 | HCID 23110281 | — |
Reaction Steps
To a solution of 317 mg di-imidazol-1-yl-methanone and 20 mg imidazole in 4 ml tetrahydrofuran a solution of 500 mg 3-(2,2-diethoxy-ethoxy)-4-methoxy-phenylamine in 2 ml tetrahydrofuran was slowly added at 0° C. After stirring at 0° C. for 1 hour 505 mg 2-methyl-2-[(quinolin-4-ylmethyl)-amino]-propionic acid methyl ester were added and the reaction mixture was allowed to warm up to room temperature. After 2 hours stirring at room temperature the solution was heated for 2 hours at 70° C. After cooling to room temperature the solvent of the mixture was removed under reduced pressure and the residue was purified by preparative HPLC (C18 reverse phase column, elution with a water/acetonitrile gradient with 0.1% trifluoroacetic acid). Lyophilization of the solution yielded a white solid. Yield: 300 mg
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759379B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-d6208bb8fe484be6a54d9580c237b667 |
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| Source note | uspto-grants-2010_07 |
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