HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 178512519, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178512548 | HCID 178512548 | — |
| Product | HCID 178512519 | HCID 178512519 | — |
Reaction Steps
The antineoplastic drug shown as Compound 1 may be synthesized as follows: p-guanidinobenzoic acid is refluxed with thionyl chloride to yield the corresponding p-guanidinobenzoic acid chloride. This is then reacted with ethyl p-hydroxybenzoylacetate in the presence of a catalyst such as dimethylaminopyridine (DMAP) to yield Compound 2 of the following structure: ##STR12##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05274162 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-ae360254d4ed46a1b21b7b99ee3aacfc |
| Source note | uspto-grants-1993_12 |