Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 4-Methoxyphenyl isothiocyanate | HCID 75293 | — |
| Reactant | Benzyl piperazine-1-carboxylate | HCID 643495 | — |
| Product | HCID 68420671 | HCID 68420671 | — |
Reaction Steps
1-Benzyloxycarbonylpiperazine (6.35 g) was dissolved in acetone (40 mL) and 4-methoxyphenyl isothiocyanate (5.19 g) were added under ice-cooling. The mixture was stirred at room temperature for 2 days. The reaction solution was concentrated under reduced pressure, and the residue was dissolved in dichloromethane (80 mL). Methyl iodide (2.7 mL) was added under ice-cooling, and the mixture was stirred at room temperature for 17 hr. The reaction solution was added to a saturated a aqueous sodium hydrogen carbonate solution, and the mixture was extracted with dichloromethane. The extract solution washed with saturated brine, dried and concentrated under reduced pressure to give 1-benzyloxycarbonyl-4-[(methylthio)(4-methoxyphenyl)iminomethyl]piperazine (12.8 g) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790725B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-e5e46b94e2c048e19ea16de161104af1 |
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| Source note | uspto-grants-2010_09 |
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