HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 2-(Methylamino)-2-oxoethyl 2-[1-(6-isobutyl-2-pyridyl)-4-piperidyl]ethylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 3-{2-[1-(6-Isobutyl-2-pyridyl)-4-piperidyl]ethyl}-1,3-oxazolidine-2,4-dione | HCID 21096968 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Methylamino)-2-oxoethyl 2-[1-(6-isobutyl-2-pyridyl)-4-piperidyl]ethylcarbamate | HCID 58861258 | — |
Reaction Steps
The process is performed according to the procedure described in Example 1 (step 1.5). Starting with 0.72 g (2.08 mmol) of 3-{2-[1-(6-isobutyl-2-pyridyl)-4-piperidyl]ethyl}-1,3-oxazolidine-2,4-dione, obtained in step 13.4, and 5.20 ml (10.40 mmol) of a solution (2M) of methylamine in tetrahydrofuran, and after chromatography on silica gel, eluting with a 95/5/0.5 mixture of dichloromethane, methanol and 28% aqueous ammonia, followed by crystallization from diisopropyl ether, 0.540 g of pure product is obtained in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08034818B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-071f92228e78403cb0ba03935c85625c |
| Source note | uspto-grants-2011_10 |