HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → 2-Bromo-5-iodoimidazo[2,1-b][1,3,4]thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 2-Bromoimidazo[2,1-b][1,3,4]thiadiazole | HCID 43667923 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Bromo-5-iodoimidazo[2,1-b][1,3,4]thiadiazole | HCID 66221540 | 89.5% |
Reaction Steps
NIS (3.83 g, 16.2 mmol, 1.1 eq) was added to a solution of 2-bromo-imidazo[2,1-b][1,3,4]thiadiazole (3.0 g, 14.7 mmol, 1 eq) in dry DMF (50 mL). The mixture was stirred at RT for 4 h and then poured into aq. Na2S2O3 (10%) and diluted with EtOAc. The organic phase was washed with water, dried and concentrated to give the desired product (pale brown solid; 4.34 g, yield 89%). 1H (300 MHz, CDCl3): δ/ppm 7.29 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08815918B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-76f3716fc2fd4185841178e892cd0f6b |
| Source note | uspto-grants-2014_08 |