HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → HCID 131710311, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | α-(Chlorocarbonyl)benzenemethanesulfonic acid | HCID 13127332 | — |
| Reactant | HCID 23620956 | HCID 23620956 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131710311 | HCID 131710311 | — |
Reaction Steps
The α-sulfo-acylamido-3-halo-cephem compounds of the Formula I wherein Q is a sulfo group (-SO3H) are prepared by following the acylation procedures employed for the preparation of α-sulfobenzylpenicillins described by U.S. Pat. No. 3,660,379 and in the J. Med. Chem., 15 (11), 11-5 (1972); ibid, p. 1108. For example, 7-amino-3-chloro-3-cephem-4-carboxylic acid is reacted with α-sulfophenylacetyl chloride in a mixture of acetone and water containing an excess of sodium bicarbonate to yield 7-(α-sulfophenylacetamido)-3-chloro-3-cephem-4-carboxylic acid. Examples of α-sulfoacylamido-3-halo-cephems of the present invention are,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04260745 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-06426f0cc2f541cf9f5aae277ada8b48 |
| Source note | uspto-grants-1981_04 |