Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 22335522 | HCID 22335522 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 9885921 | HCID 9885921 | 54% |
Reaction Steps
A mixture of (±)-(E)-N-[4-[1-(1H-imidazol-1-yl)-2-methylpropyl]phenyl]-2-[(4-nitrophenyl)-methylene]propanamide (0.00742 mol) in THF (80 ml) and TiCl3 (30 ml) was stirred at 0° C. for 15 minutes. The mixture was poured into water, ice and NaOH 3N and extracted with CH2Cl2 (2×100 ml). The combined organic layers were dried, filtered and the solvent evaporated. The residue was taken up in CH2Cl2 and (C2H5)2O. The precipitate was filtered off and stirred K2CO3 10% and CH2Cl2, dried, filtered off and evaporated. The residue was crystallized from 2-propanone. The precipitate was filtered off, taken up in Na2CO3 10% and CH2Cl2. The organic layer was dried, filtered off and evaproated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 96/4/0.1). The pure fractions were collected and evaporated. The residue was crystallized from (C2H5)2O, yielding 1.5 g (±)-(E)-2-[(4-aminophenyl)methylene]-N-[4-[1-(1H-imidazol-1-yl)-2-methylpropyl]phenyl]propanamide (compound 611).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07179825B2 |
|---|
| Source dataset | uspto-grants-2007_02 |
|---|
| ORD ID | ord-e4d526a219e54447baf9a63bc353c9a4 |
|---|
| Source note | uspto-grants-2007_02 |
|---|