HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873225Generated: November 2, 2026
2-Mercaptobenzoic Acid → HCID 15480017, compound
https://huagongshe.com/reaction/1873225
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Mercaptobenzoic Acid | HCID 5443 | — |
| Reactant | Zaltoprofen | HCID 5720 | — |
| Reactant | HCID 11138738 | HCID 11138738 | — |
| Product | HCID 15480017 | HCID 15480017 | — |
Reaction Steps
Preparation-III of the invention for preparing Zaltoprofen is characterized in that 2-(4-amino-3-carboxymethylphenyl)propionic acid or its salt is diazotized and then reacted with thiosalicylic acid to give 2-[3-carboxymethyl-4-(2-carboxyphenylthio)phenyl]propionic acid or its salt; the resulting compound is esterified to give 2-[3-(lower)alkoxycarbonylmethyl-4-(2-(lower)alkoxycarbonylphenylthio)phenyl]propionic acid (lower)alkyl ester; the resulting ester is subjected to cyclization reaction, to give 2-(10,11-dihydro-11-(lower)alkoxycarbonyl-10-oxodibenzo[b,f]thiepin-2-yl)propionic acid (lower)alkyl ester; and the resulting ester is finally subjected to hydrolysis and decarboxylation. Preparation-III is illustrated in the following reaction scheme III: ##STR9## 1) Preparation of 2-[3-carboxymethyl-4-(2-carboxyphenylthio)phenyl]propionic acid or its salt
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06111115 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-d7f5467535144052906d022b74707f45 |
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| Source note | uspto-grants-2000_08 |
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