Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 22662739 | HCID 22662739 | — |
| Reactant | 4-Piperidinylmethyl 4-amino-5-chloro-2-methoxybenzoate | HCID 22662757 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22662758 | HCID 22662758 | 26% |
Reaction Steps
A mixture of 1-chloro-(4-fluorophenoxy)propane (2.3 g), intermediate 11 (3 g) and N,N-diethylethanamine (2.8 ml) in DMF (50 ml) was stirred for 48 hours at 70° C. The reaction mixture was cooled and the solvent was evaporated. The residue was partitioned between DCM and water. The organic layer was separated, washed with water, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH 95/5). The pure fractions were collected and the solvent was evaporated. The residue was crystallized from ACN (0° C.). The precipitate was filtered off and dried (vacuum; 50° C.), yielding 1.17 g (26%) [1-[3-(4-fluorophenoxy)propyl]-4-piperidinyl]methyl 4-amino-5-chloro-2-methoxybenzoate (compound 1, mp. 140.0° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06800628B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-a1f4f59beea84b7a9e6172d00909172b |
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| Source note | uspto-grants-2004_10 |
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