Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl isocyanate | HCID 76639 | — |
| Reactant | HCID 2410357 | HCID 2410357 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 27533560 | HCID 27533560 | 47.5% |
Reaction Steps
To a solution of 1-(4-Nitro-benzenesulfonyl)-piperazine (1.0 g, 2.6 mmol) in pyridine (10 ml) was added benzyl isocyanate (0.35 ml, 2.85 mmol) in one portion. The resulting mixture was then heated at 50° C. for 2 hours before being cooled to room temperature and concentrated under vacuum. The resulting residue was dissolved in ethyl acetate (50 ml) and washed with 1M HCl (100 ml), the organic layer was separated, dried (MgSO4), filtered and concentrated under vacuum to give the title compound (0.5 g, 47% yield) as a yellow solid which was used without further purification. Tr=1.86 min, m/z (ES+) (M+H)+ 405.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946197B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-b6a90d854fe64ae191b9d99af008d299 |
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| Source note | uspto-grants-2015_02 |
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