Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid | HCID 392871 | — |
| Reactant | tert-Butyl 4-(2-Bromoacetyl)piperidine-1-carboxylate | HCID 18187487 | — |
| Reactant | HCID 86640987 | HCID 86640987 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86640988 | HCID 86640988 | 94% |
Reaction Steps
1-(5-Bromo-4-(2-methylpyridin-3-yloxy)pyridin-2-yl)thiourea (1.48 g, 4.4 mmol), tert-butyl 4-(2-bromoacetyl)piperidine-1-carboxylate (1.41 g, 4.60 mmol, prepared from 1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid utilizing the procedure from Example 1, steps A-C), and triethylamine (0.93 mL, 6.56 mmol) were diluted in ethanol (130 mL). The reaction was stirred at 70° C. overnight and then concentrated. Water was added and the solution was extracted with ethyl acetate, dried and concentrated to give the title compound (2.37 g, 94% yield) as light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431713B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-d217b59498ac4072905e555dea0b5de5 |
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| Source note | uspto-grants-2013_04 |
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