HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-4-Methyloxazolidin-2-one → (R)-3-{4-[4-(5-cyano-3-methylpyridin-2-yl)piperazine-1-carbonyl]-3-methylphenyl}-4-methyloxazolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-4-Methyloxazolidin-2-one | HCID 2734858 | — |
| Reactant | 6-[4-(4-Bromo-2-methylbenzoyl)piperazin-1-yl]-5-methylnicotinonitrile | HCID 58484676 | — |
| Product | (R)-3-{4-[4-(5-cyano-3-methylpyridin-2-yl)piperazine-1-carbonyl]-3-methylphenyl}-4-methyloxazolidin-2-one | HCID 58484809 | 65.7% |
Reaction Steps
By reaction and treatment in the same manner as in Example 1 and using 6-[4-(4-bromo-2-methylbenzoyl)piperazin-1-yl]-5-methylnicotinonitrile (210 mg) described in Preparation Example 133 and (R)-4-methyloxazolidin-2-one (80 mg) described in Preparation Example 25, the title compound (145 mg) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354401B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-53f0ec013153455b804df5050dd25ef5 |
| Source note | uspto-grants-2013_01 |