HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanethiol → HCID 70615406, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | HCID 70615973 | HCID 70615973 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70615406 | HCID 70615406 | — |
Reaction Steps
2,2,2-Trichloroethyl 3-bromomethyl-7β-phenoxyacetamidoceph-3-em-4-carboxylate, 1β-oxide (11.48g, 20 mmole) was reacted with methanethiol as in Example D18(i) and the resulting solution in N,N-dimethylformamide used directly in a reduction step as described in Example D18(ii) to provide the solvated title compound as a pale-yellow foam (10.90 g,), [α]D + 37.5° (c, 1.25) λmax. 269 nm (E1cm1% 165) and 276 nm. (E1cm1% 160) inflexion at 263 nm (E1cm1% 151). The P.M.R. spectrum of this product closely resembled that of the product from Example D18(ii)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04113591 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-c1d3dd03d4e34b2eade7499b24cb5158 |
| Source note | uspto-grants-1978_09 |