HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methoxyethylamine → tert-Butyl 4-[(2-methoxyethyl)amino]piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methoxyethylamine | HCID 8018 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyl 4-[(2-methoxyethyl)amino]piperidine-1-carboxylate | HCID 43652134 | — |
Reaction Steps
Amine preparation: 1-BOC-4-piperidone (500 mg) and 2-methoxyethylamine 218 μL) were stirred in MeOH at room temperature. After 16 h, sodium borohydride was added (190 mg) carefully. After a further 3 h, the reaction mixture was diluted with DCM, washed with water, dried (MgSO4) and the solvent removed in vacuo to yield 4-(2-methoxy-ethylamino)-piperidine-1-carboxylic acid tert-butyl ester (560 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946217B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-9e43554cb8e74e05aee80b428bbc910c |
| Source note | uspto-grants-2015_02 |