Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(1-t-Butoxycarbonyl-2-methylpiperidin-4-yloxy)-3-chloronitrobenzene | HCID 22181217 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 22180993 | HCID 22180993 | 90.6% |
Reaction Steps
To a suspension of 4-(1-t-butoxycarbonyl-2-methylpiperidin-4-yloxy)-3-chloronitrobenzene (1.15 g) obtained in reference example 85 in 90% formic acid (3.10 g) was added 37% formaldehyde (2.50 g), and the resulting mixture was stirred at 100° C. for 2 hours. After cooling to room temperature, the reaction mixture was neutralized with an aqueous potassium carbonate solution and extracted with ethyl acetate. The extract was washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue obtained was purified by chromatography on a silica gel column using a mixed solvent of dichloromethane and methanol (9:1) as the eluent to afford the title compound (0.80 g, yield: 90%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030138B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-deb1478bca3c4802b12a68bd2d9e8727 |
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| Source note | uspto-grants-2006_04 |
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