HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → tert-butyl N-[[1-[(E)-N'-hydroxycarbamimidoyl]piperidin-4-yl]methyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | tert-butyl N-[(1-cyanopiperidin-4-yl)methyl]carbamate | HCID 23396324 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | tert-butyl N-[[1-[(E)-N'-hydroxycarbamimidoyl]piperidin-4-yl]methyl]carbamate | HCID 178453097 | — |
Reaction Steps
(1-Cyano-piperidin-4-ylmethyl)-carbamic acid tert-butyl ester (2 g, 8.36 mmol), hydroxylamine hydrochloride (3.48 g, 50.14 mmol) and triethylamine (5.92 g, 58.5 mmol) were stirred in 30 ml of isopropanol at room temperature for 4 hours. The mixture was evaporated. After addition of water (pH4) and ethyl acetate, the organic layer was separated and evaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067665B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-ecba89ba85b740ff8bc5e1b26c10e478 |
| Source note | uspto-grants-2006_06 |