Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | HCID 11010206 | HCID 11010206 | — |
| Product | HCID 19837972 | HCID 19837972 | — |
Reaction Steps
To an ice-cooled solution of a mixture of 6-chloro-1-carboxymethyl-2-oxo-1,2-dihydrothiazolo[5,4-b]pyridine (3.47 g) and N-hydroxysuccinimide (1.96 g) in N,N-dimethylformamide (20 ml) was gradually added N,N-dicyclohexylcarbodiimide (3.51 g). The mixture was stirred for 1 hour at ambient temperature and dicyclohexylurea that precipitated from the reaction mixture was removed by filtration. To a solution of piperazine (6.11 g) in N,N-dimethylformamide (80 ml) was added dropwise the filtrate for a period of 1.5 hours below 20° c. The final mixture was stirred for 4 hours at ambient temperature, and then filtered. The filtrate was concentrated under reduced pressure below 50° C. and the residue was dissolved in 2N hydrochloric acid. The aqueous solution was washed with chloroform and then adjusted to pH 9 with an aqueous solution of sodium hydrogen carbonate. The turbid solution was extracted with chloroform, and the extract was dried over magnesium sulfate and concentrated under reduced pressure to give a white powder of 6-choro-2-oxo-1-[(1-piperazinyl)carbonylmethyl]-1,2-dihydrothiazolo[5,4 -b]pyridine (3.24 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04797399 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-091ec2f0ad2445b4ba6b64880afa5eb4 |
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| Source note | uspto-grants-1989_01 |
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