Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Heptanamine | HCID 8127 | — |
| Reactant | HCID 67147910 | HCID 67147910 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67147907 | HCID 67147907 | 50% |
Reaction Steps
70 μl (0.45 mmol) of heptylamine are added to a solution of 110 mg (0.25 mmol) of methyl 2(S)-ethoxy-3-(6-{3-[methyl(4-nitrophenoxycarbonyl)amino]phenyl}pyrid-3-yl)propanoate in 3 ml of dimethylformamide. The reaction medium is heated at 80° C. for 3 hours. After addition of water, the reaction medium is extracted with ethyl acetate. The organic phase is dried over magnesium sulfate, filtered and evaporated. The residue obtained is purified by thin-layer chromatography on silica eluted with a 6/4 and then 5/5 heptane/ethyl acetate mixture. 50 mg (50%) of methyl 2(S)-ethoxy-3-{6-[3-(3-heptyl-1-methylureido)phenyl]pyrid-3-yl}propanoate are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07625914B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-b47ab426b311445caff2b49855bd621d |
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| Source note | uspto-grants-2009_12 |
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