HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665129Generated: October 30, 2026
Dimethylformamide → HCID 178508756, compound
https://huagongshe.com/reaction/1665129
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 178451396 | HCID 178451396 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178508756 | HCID 178508756 | — |
Reaction Steps
Iodotrimethylsilane (0.23 ml, 1.66 mmol) is added to a suspension of (E)-tert-Butyl 2′-(3,5-diamino-6-chloropyrazine-2-carbonylimino)-8-azaspiro[bicyclo[3.2.1]octane-3,4′-imidazolidine]-8-carboxylate (Ex. 251) (500 mg, 1.11 mmol) in DCM (10 ml). DMF (5 ml) is then added and the reaction is stirred at room temperature overnight. Iodotrimethylsilane (0.5 ml) is added and the reaction mixture is concentrated in vacuo. The yellow solid is suspended in DCM and collected by filtration. The solid is dissolved in 1:1 MeOH/DCM and loaded onto an SCX-2 cartridge eluted with DCM followed by MeOH and NH3/MeOH. The methanolic ammonia fractions are concentrated in vacuo to afford (E)-3,5-diamino-6-chloro-N-(8-azaspiro[bicyclo[3.2.1]octane-3,4′-imidazolidine]-2′-ylidene)pyrazine-2-carboxamide as a yellow gum; [M+H]+ 351
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08039472B2 |
|---|
| Source dataset | uspto-grants-2011_10 |
|---|
| ORD ID | ord-79ed563614fb4ca0a4aaed0a23263a3d |
|---|
| Source note | uspto-grants-2011_10 |
|---|