HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728133Generated: October 30, 2026
Potassium Carbonate → HCID 9972556, compound
https://huagongshe.com/reaction/728133
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium thiocyanate | HCID 15666 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 10083527 | HCID 10083527 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 9972556 | HCID 9972556 | 14% |
Reaction Steps
A solution of 2-[2-(4-aminophenyl)ethyl]-7-methylimidazo[1,2-a]pyridine (2.5 g) and ammonium thiocyanate (1.5 g) in acetic acid (25 ml) was stirred at ambient temperature for 1 hour. A solution of bromine (0.6 ml) in acetic acid (3 ml) was dropwise added thereto at 15° to 18° C. under stirring and the resulting mixture was stirred at 10° to 20° C. for 1 hour. A mixture of ethyl acetate and water was added to the reaction mixture and the mixture was adjusted to pH 7.5 with potassium carbonate. The separated organic layer was washed with brine and dried over magnesium sulfate. The crude product obtained by concentration was purified by silica gel column chromatography eluting with a mixture of chloroform and methanol (19:1 V/V). The eluted fractions containing desired product were evaporated to give 6-[2-(7-methylimidazo[1,2-a]pyridin-2-yl)ethyl]-2-aminobenzothiazole (0.43 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05047411 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-5be07352805b4300930c3ca073f50a4e |
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| Source note | uspto-grants-1991_09 |
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