Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 18510678 | HCID 18510678 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18510705 | HCID 18510705 | 68% |
Reaction Steps
) A solution of chloroacetylchloride (0.0089 mol) in CH2Cl2 (20 ml, dried over MgSO4) was added to a cooled solution of (±)-N-[4-(aminophenylmethyl)phenyl]4,5-dihydro-3-(3-pyridinyl)-5-isoxazolecarboxamide(0.0081 mol) and N-ethyl-N-(1-methylethyl)-2-propanamine (0.0093 mol) in CH2Cl2 (100 ml). The reaction mixture was stirred for one hour at 0° C. Water was added. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated under reduced pressure. The residue (crude oil) was purified by short column chromatography over silica gel (eluent: CH2Cl2/CH3OH 98/2). The pure fractions were collected and the solvent was evaporated under reduced pressure. The residue was stirred in EtOAc. The precipitate was filtered off, washed with EtOAc, and dried, yielding 2.47 g (68%) of (±)-N-[4-[[(chloroacetyl)amino]phenylmethyl]phenyl]4,5-dihydro-3-(3-pyridinyl)-5-isoxazolecarboxamide. (compound 127)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07414048B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-7775c69ecb904d67814be4e58bf2a4b2 |
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| Source note | uspto-grants-2008_08 |
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