HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(2-Bromoethyl)indole → 3-(2-Bromoethyl)-1-(6-chloroimidazo[2,1-b]thiazole-5-sulfonyl)indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(2-Bromoethyl)indole | HCID 76924 | — |
| Reactant | 6-Chloroimidazo(2,1-b)(1,3)thiazole-5-sulfonyl chloride | HCID 2799717 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(2-Bromoethyl)-1-(6-chloroimidazo[2,1-b]thiazole-5-sulfonyl)indole | HCID 11259349 | 58% |
Reaction Steps
A mixture of 3-(2-bromoethyl)indole (1.0 g, 4.46 mmol) and 6-chloroimidazo[2,1-b]thiazole-5-sulfonyl chloride (0.96 g, 1.1 eq.) in THF is treated with potassium t-butoxide (0.48 g, 1.1 equiv.) at room temperature, stirred for 16 h, quenched with saturated NaHCO3 and extracted with EtOAc. The extracts are combined, dried over MgSO4 and concentrated in vacuo to give the title product as a brown oil, 1.2 g (58% yield), identified by HPLC and mass spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06770642B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-1c31d52117e2466ea1e8d202eb25264e |
| Source note | uspto-grants-2004_08 |