Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 66990568 | HCID 66990568 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66991028 | HCID 66991028 | — |
Reaction Steps
Acetic acid (0.12 mL), a 37% aqueous solution of formaldehyde (0.10 mL), and sodium triacetoxyborohydride (0.54 g) were sequentially added to a tetrahydrofuran (5.4 mL) solution of the obtained methyl 2-(2-(benzyloxy)-5-(piperidin-4-yl)benzamido)-4-bromobenzoate (0.54 g), followed by stirring at room temperature for 1 hour. The solvent was evaporated under reduced pressure, and a saturated aqueous solution of sodium bicarbonate and ethyl acetate were added to the residue. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [eluent: 100-90% chloroform/methanol] to obtain 0.48 g of methyl 2-(2-(benzyloxy)-5-(1-methylpiperidin-4-yl)benzamido)-4-bromobenzoate as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492582B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-1c75b786c2784372a453e5f42e2e3d3d |
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| Source note | uspto-grants-2013_07 |
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