HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → (5R)-3-[3-Fluoro-4-(1,2,3,6-tetrahydropyridin-4-yl)phenyl]-5-[(4-methyl-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | (5R)-3-[4-(1-Benzyl-1,2,3,6-tetrahydropyridin-4-yl)-3-fluorophenyl]-5-[(4-methyl-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one | HCID 10366343 | — |
| Reactant | HCID 68879337 | HCID 68879337 | — |
| Product | (5R)-3-[3-Fluoro-4-(1,2,3,6-tetrahydropyridin-4-yl)phenyl]-5-[(4-methyl-1,2,3-triazol-1-yl)methyl]oxazolidin-2-one | HCID 57526968 | 107.4% |
Reaction Steps
(5R)-3-[4-(1-Benzyl-1,2,3,6-tetrahydropyridin-4-yl)-3-fluorophenyl]-5-[(4-methyl-1H-1,2,3-triazol-1-yl)methyl]-1,3-oxazolidin-2-one (Example 43) (5.13 g, 11.46 mmol) was reacted with diisopropylethylamine (0.40 ml, 2.29 mmol) and 1-chloroethylchloroformate (1.50 ml, 13.76 mmol) as described for Intermediate 53 to give the crude title compound (4.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07473699B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-77b14928992d4f1cb318a0f8efbcc46e |
| Source note | uspto-grants-2009_01 |