HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → HCID 54403077, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Benzene, (diazomethyl)- | HCID 136601 | — |
| Reactant | HCID 15004125 | HCID 15004125 | — |
| Reactant | HCID 54056417 | HCID 54056417 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 54403077 | HCID 54403077 | — |
Reaction Steps
The resulting (R)-1,4-dihydro-2,6-dimethyl-1-methoxymethyl-4-(3-nitrophenyl)5-pivaloyloxymethoxycarbonyl -3-pyridinecarboxylic acid was treated with a 0.5 M solution of diazomethane in diethyl ether and then treated with a 10% potassium hydroxide solution in methanol. The resulting (S) -1,4-dihydro-2,6-dimethyl-1-methoxymethyl-4-(3-nitrophenyl)-5-methoxycarbonyl-3-pyridinecarboxylic acid (recrystallized) was reacted with phenyldiazomethane to obtain (R)-benzyl methyl 1,4-dihydro-2,6-dimethyl-1-methoxymethyl-4-(3-nitrophenyl)-3,5-pyridinedicarboxylate. As a result of HPLC (isopropanol/hexane=1/10) using CHIRALCEL OD, the optical purity was found to be 69% ee.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05234821 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-57644a4422cb4820bde4deb3cabbd807 |
| Source note | uspto-grants-1993_08 |