HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-morpholine-3-carboxylic acid → (3S)-4-((5-(ethoxycarbonyl)-6-(5-fluoro-4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)morpholine-3-carboxyli c acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-morpholine-3-carboxylic acid | HCID 1501894 | — |
| Reactant | HCID 118107602 | HCID 118107602 | — |
| Product | (3S)-4-((5-(ethoxycarbonyl)-6-(5-fluoro-4'-(trifluoromethyl)-[1,1'-biphenyl]-2-yl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)morpholine-3-carboxyli c acid | HCID 73295974 | 50% |
Reaction Steps
Ethyl 6-(bromomethyl)-4-(5-fluoro-4′-(trifluoromethyl)-[1,1′-biphenyl]-2-yl)-2-(thiazol-2-yl)-1,4-dihydropyrimidine-5-carboxylate (3 g, 5.3 mmol) was reacted with (S)-morpholine-3-carboxylic acid (0.69 g, 5.3 mmol) according to the procedure as described in Example 1, Step C to give the title compound as a yellow solid (1.64 g, 50%). The compound was characterized by the following spectroscopic data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340538B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-22f00e607e8e44fd86ea8fe20afca747 |
| Source note | uspto-grants-2016_05 |