HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 131710482, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 53628223 | HCID 53628223 | — |
| Reactant | HCID 131710483 | HCID 131710483 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 131710482 | HCID 131710482 | — |
Reaction Steps
7-Cyanomethylthioacetamido-3-methoxy-3-cephem-4-carboxylic acid (35 mg.) is dissolved in 1 ml. of methanol and 50 μ l of 2.5 M potassium 2-ethyl hexanoate is added. Addition of ether causes precipitation of a very hygroscopic solid. All solvent is removed in vacuo from the mixture and the residue is solidified by the addition of acetonitrile. The desired potassium salt is collected by filtration and dried yielding 19 mg; NMR (DMSO d6 δ) 3.43 (m, CH2),3.52 (s, NCCH2SCH2CO--) 3.76 (s,OCH3), 4.10 (d, J=4Hz, H6), 5.30 (q, J=4, 9.5 Hz, H7), 9.03 (d, J=9.5 Hz,NH); νmax (KBr) 3575, 3270, 2240, 1750, 1630, 1595, 1540 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03985746 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-6b87ab3dfa1943b58161ec8bad1aab40 |
| Source note | uspto-grants-1976_10 |