Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | HCID 19802733 | HCID 19802733 | — |
| Reactant | HCID 53791839 | HCID 53791839 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19802764 | HCID 19802764 | 37% |
Reaction Steps
To a solution of 43.2 mg (0.175 mmol) of ethyl valerate benzoylhydrazone (from Step K) in 0.2 ml of ethanol was added a solution of 82 mg (0.262 mmol) of methyl 2-(4-aminomethyl-2-propylphenoxy)-2-phenylacetate (from Step J) in 0.2 ml of ethanol. The resulting solution was stirred under N2 at 50° C. for 5.5 hours. After dilution with 0.4 ml of ethanol, the solution was then stirred at 70° C. under a condenser for 13 hours. Next, the solution was co-evaporated with CHCl3. The residue was chromatographed twice in silica gel columns (gradient elution, first with 0.5-3% and then with 0.3-2% MeOH in CHCl2) to give 32 mg (37%) of the title compound as a white glass; homogeneous by TLC in 9:1 CH2Cl2 -MeOH.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05177095 |
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| Source dataset | uspto-grants-1993_01 |
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| ORD ID | ord-d81119bf06f64e27b0a1c8b1d9db004f |
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| Source note | uspto-grants-1993_01 |
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