HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36910Generated: October 23, 2026
alpha-chloro-N,N-dimethyl-2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetamide hydrochloride → N,N-dimethyl-2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetamide
https://huagongshe.com/en/reaction/36910
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | alpha-chloro-N,N-dimethyl-2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetamide hydrochloride | HCID 19936712 | — |
| Reactant | Sodium Formaldehyde Sulfoxylate | HCID 23689980 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N,N-dimethyl-2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetamide | HCID 19936717 | — |
Reaction Steps
34 g (0.077 mole) of α-chloro-N,N-dimethyl-2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetamide hydrochloride in solution in 500 ml of dichloromethane are treated with 36.9 g (0.24 mole) of Rongalite®, while stirring the mixture at room temperature for 24 h. The organic phase is separated after settling has taken place, the solid residue is washed with dichloromethane, the organic phase is washed with a saturated sodium hydrogen carbonate solution and then with water, it is dried over sodium sulphate, the solvent is evaporated under reduced pressure and 22 g of solid are obtained. After recrystallization from ethanol and treatment with vegetable black, 17 g of pale yellow crystals are finally obtained. Melting point: 194°-195° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05418248 |
|---|
| Source dataset | uspto-grants-1995_05 |
|---|
| ORD ID | ord-d92df32fa3c24976935b2b186cc36c14 |
|---|
| Source note | uspto-grants-1995_05 |
|---|