HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004849Generated: October 30, 2026
Acetic Acid → (S)-(-)-N-[[3-[4-[1-(4-Oxo-2-thiazolinyl)-4-piperidinyl]-3-fluorophenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide
https://huagongshe.com/reaction/1004849
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methyl 2-thiocyanatoacetate | HCID 12718 | — |
| Reactant | (S)-(-)-N-[[2-Oxo-3-[4-(4-piperidinyl)-3-fluorophenyl]-5-oxazolidinyl]methyl]acetamide | HCID 15887422 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-(-)-N-[[3-[4-[1-(4-Oxo-2-thiazolinyl)-4-piperidinyl]-3-fluorophenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide | HCID 69765548 | — |
Reaction Steps
A mixture of (S)-(-)-N-[[2-oxo-3-[4-(4-piperidinyl)-3-fluorophenyl]-5-oxazolidinyl]methyl]acetamide (EXAMPLE 20, 310 mg), methyl thiocyanatoacetate (121 mg, Bull. Chem. Soc. Jpn. 1972, 45(5), 1507) and glacial acetic acid (55 mg) in absolute ethanol (5 mL) is stirred at reflux under N2 for 4 hrs and then cooled to ambient temperature, diluted with methylene chloride (45 mL), washed with water (2×15 mL) and saline (20 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue is chromatographed on silica gel (230-400 mesh, 45 g), eluting with methanol/methylene chloride (4/96), and those fractions with an Rf =0.47 by TLC (methanol/chloroform, 10/90) are pooled and concentrated to give the title compound, mp 222-224° C. (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06051716 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-aac9769d6c4b4a42917c014de1a681d6 |
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| Source note | uspto-grants-2000_04 |
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