HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 3-Iodo-2,6-dimethyl-8-(1-propyl-butyl)-imidazo[1,2-b]pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 2,6-Dimethyl-8-(1-propyl-butyl)-imidazo[1,2-b]pyridazine | HCID 68840997 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Iodo-2,6-dimethyl-8-(1-propyl-butyl)-imidazo[1,2-b]pyridazine | HCID 57932906 | 99.8% |
Reaction Steps
In an oven dried nitrogen purged 25 mL round bottom flask, 0.088 g (0.359 mmol) of 2,6-Dimethyl-8-(1-propyl-butyl)-imidazo[1,2-b]pyridazine, in 5 mL of dry acetonitrile is cooled to 0 C. 0.0.81 g (0.359 mmol) of NIS is added and the bath is allowed to expire. TLC in 1:1 Hexanes:Ethyl Acetate indicates SM is gone. Remove solvents to obtain 0.133 g of the title compound, quantitative yield. MS; 1H NMR (DMSO-d6)=6.985 (s, 1H); 3.262-3.190 (m, 1H); 2.502 (s, 3H); 2.480 (s, 3H); 1.823-1.600 (m, 4H); 1.182-0.985 (m, 4H); 0.804-0.768 (m, 6H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07557103B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-a0175cd7528447278ed8a5c89a0f9fc0 |
| Source note | uspto-grants-2009_07 |