HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989868Generated: October 30, 2026
Ammonium Chloride → 5-Cyano-7-methylthioimidazo[5,1-b]thiazole
https://huagongshe.com/reaction/989868
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | p-Toluenesulphonyl cyanide | HCID 87946 | — |
| Reactant | HCID 23449208 | HCID 23449208 | — |
| Reactant | HCID 178420660 | HCID 178420660 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Cyano-7-methylthioimidazo[5,1-b]thiazole | HCID 23449220 | 49.1% |
Reaction Steps
A 1 M ethylmagnesium bromide/THF solution (2.0 ml) was added in an argon atmosphere at −40° C. to a solution of 405 mg of 5-iodo-7-methylthioimidazo[5,1-b]thiazole in 12 ml of dry THF. The mixture was stirred at the same temperature for 30 min. p-Toluenesulfonyl cyanide (372 mg) was added thereto. The temperature of the system was raised to −5° C. over a period of one hr. A saturated aqueous ammonium chloride solution was added to the reaction mixture. Ethyl acetate was added thereto, followed by washing with saturated brine. The organic layer was dried over anhydrous magnesium sulfate. The solvent was removed by distillation. The residue was purified by column chromatography on silica gel (dichloromethane:ethyl acetate:hexane=3:1:1) to give 131 mg of 5-cyano-7-methylthioimidazo[5,1-b]thiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458780B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-2e3ad34fde524f83863269ae092ce735 |
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| Source note | uspto-grants-2002_10 |
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