HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl isocyanate → N-(1-Boc-piperidin-3-yl-methyl)-N-phenyl-N'-ethylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl isocyanate | HCID 8022 | — |
| Reactant | N-(1-Boc-piperidin-3-ylmethyl)aniline | HCID 12972131 | — |
| Product | N-(1-Boc-piperidin-3-yl-methyl)-N-phenyl-N'-ethylurea | HCID 12972132 | 95% |
Reaction Steps
To a solution of N-(1-Boc-piperidin-3-ylmethyl)aniline 1 (102 mg, 0.35 mmol) in 1 mL of dry CH2Cl2was added ethyl isocyanate (95%, 35 μL, 1.2 eq.) at room temperature. After being shaken at room temperature for overnight, the reaction mixture was passed through an aminopropyl NH2 cartridge and washed with CH2Cl2. Removal of the CH2Cl2 afforded N-(1-Boc-piperidin-3-yl-methyl)-N-phenyl-N′-ethylurea (2) (120 mg, 95%). LRMS 285 (M-100)+ 261.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06476050B2 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-edf865da5b9a422baf18473828b938ac |
| Source note | uspto-grants-2002_11 |