Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 22473634 | HCID 22473634 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22473769 | HCID 22473769 | — |
Reaction Steps
Bromine (0.16 ml) was added dropwise at 0-5° C. over 5 minutes to a stirred solution of 3-(benzo[b]thiophen-4-yl)-5,6-dihydroimidazo[2,1-b]thiazole (0.8 g; prepared by basification of 1 g of the hydrochloride salt described in Example 2) in dichloromethane (50 ml), then the mixture was stirred at 0° C. for 10 minutes and at ambient temperature for 1.5 hours. The resulting solid was collected by filtration, washed with dichloromethane (30 ml) and dried in vacuo at 60° C. to give 3-(benzo[b]thiophen-4-yl)-2-bromo-5,6-dihydroimidazo[2,1-b]thiazole hydrobromide (1.28 g) as a pale yellow solid which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06900216B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-4e20bcdb98f947e7bb5b559ca9f817f8 |
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| Source note | uspto-grants-2005_05 |
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