HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosulfamic acid → 3-(Aminosulfonyl)aminomethylimidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosulfamic acid | HCID 24499 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Aminomethylimidazo[5,1-b]thiazole | HCID 19605155 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(Aminosulfonyl)aminomethylimidazo[5,1-b]thiazole | HCID 19605164 | — |
Reaction Conditions
| Temperature | -25 °C |
|---|
Reaction Steps
A 770 mg potin of 3-aminomethylimidazo[5,1-b]thiazole was dissolved in 15 ml of DMF, and 4.78 ml of N,N-diisopropylethylamine and 1.04 g of sulfamoyl chloride were further added at -60° C., followed by stirring at -30 to -20° C. for 4 hours. The reaction solution was concentrated under reduced pressure and then dissolved in 30 ml of water, and the solution was adjusted to pH 7.5 with an aqueous sodium hydrogencarbonate solution. After purification by Diaion HP-20 Resin, crystallization was carried out from methanol to obtain 636 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05990101 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-5ccbb9ab523f476e8bb9fe9ba7d8887c |
| Source note | uspto-grants-1999_11 |