HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863827Generated: October 26, 2026
Hydrogen Sulfide → 3-p-Amidinophenyl-5-(p-methoxycarbonylmethylphenoxymethyl)oxazolidin-2-one
https://huagongshe.com/reaction/863827
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 3-p-Cyanophenyl-5-(p-methoxycarbonyimethylphenoxymethyl)oxazolidin-2-one | HCID 15281528 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 3-p-Amidinophenyl-5-(p-methoxycarbonylmethylphenoxymethyl)oxazolidin-2-one | HCID 19356317 | — |
Reaction Steps
H2S gas is passed, at -10°, into a solution of 1.2 g of 3-p-cyanophenyl-5-(p-methoxycarbonylmethylphenoxymethyl)oxazolidin-2-one (obtainable in accordance with Example 1) in 50 ml of pyridine and 7 ml of triethylamine. The mixture is subsequently stirred at room temperature for 14 h and concentrated by evaporation; the residue is dissolved in 50 ml of acetone and treated with 9 ml of methyl iodide. After this mixture has been stirred for a further 6 h, it is filtered and the residue is washed with 5 ml of acetone and dissolved in 30 ml of methanol; 4.6 g of ammonium acetate are added to this solution, which is stirred at room temperature for 24 h. Following the customary working-up, 3-p-amidinophenyl-5-(p-methoxycarbonylmethylphenoxymethyl)oxazolidin-2-one (semihydriodide) is obtained, M.p. 151°-152°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05561148 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-03d0ad62c325426d82d98e44d924df30 |
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| Source note | uspto-grants-1996_10 |
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