Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | HCID 59178824 | HCID 59178824 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59178925 | HCID 59178925 | — |
Reaction Steps
The 1-chloroacetone (57 mg, 0.61 mmol) and tert-butyl 1′-(aminocarbonothioyl)-4,4′-bipiperidine-1-carboxylate (prepared as for Example 175, step 1) (200 mg, 0.61 mmol) were dissolved in ethanol (1.2 ml) and heated at 75° C. overnight. The solution was cooled to RT, and the solvent removed in vac. The residue was used in the subsequent procedure without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445499B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-31c41f40ee214fba94fe497b4950d38a |
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| Source note | uspto-grants-2013_05 |
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