Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | HCID 67055698 | HCID 67055698 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86646168 | HCID 86646168 | — |
Reaction Steps
To a suspension of trichloromethyl chloroformate (0.15 ml) and O,N-dimethylhydroxyamine hydrochloride (0.24 g) in methylene chloride (10 ml) was added TEA (1.02 ml) at room temperature, and the mixture was stirred for 1 hour. The suspension was added dropwise to a solution of (S)-4-amino-5-chloro-2-ethoxy-N-[[4-(4-piperidinylmethyl)-2-morpholinyl]methyl]benzamide (Example 26) (1.0 g) in methylene chloride (10 ml) under ice cooling. After completion of addition, the internal temperature of the reaction solution was warmed to room temperature, and the solution was stirred for 2 hours. The reaction solution was washed with water, then brine, and then dried over anhydrous magnesium sulfate. The solvent was removed in vacuo. The residue was purified by silica gel column chromatography (eluent: chloroform/methanol=10/1) to give the titled compound (0.8 g) as a white solid. Melting point 127-129° C. (recrystallized from EA/H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906510B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-e9d0e8977efa41d7a45e77990d2c127f |
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| Source note | uspto-grants-2011_03 |
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