HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → alpha-[(5-Chlorothiazolo[5,4-b]pyridin-2-yl)thio]alpha-phenyl acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Bromo(phenyl)acetic acid | HCID 97919 | — |
| Reactant | HCID 178527792 | HCID 178527792 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | alpha-[(5-Chlorothiazolo[5,4-b]pyridin-2-yl)thio]alpha-phenyl acetic acid | HCID 20249365 | 74.3% |
Reaction Steps
A methylene chloride solution of 4.05 g (0.02 m) 5-chloro-2-mercaptothiazolo[5,4-b]pyridine, 4.30 g (0.02 m) α-bromophenylacetic acid and 4.0 g (0.04 m) triethylamine is heated to gentle reflux overnight. The methylene chloride solution is extracted twice with a dilute hydrochloric acid solution and once with water and then dried over anhydrous MgSO4. After the solvent is removed, the residual solid is recrystallized from acetonitrile. 5.0 g (74% yield) of title compound, melting at 175°-7° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04367233 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-482b3cdb39a34cfebcdc1215fa3d6dab |
| Source note | uspto-grants-1983_01 |