HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 1-(2-Chloro-5-thiazolylmethyl)-3,3-dimethyl-l-methanesulphonyl-2-nitroguanidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | N-(2-chloro-5-thiazolylmethyl)-N',N'-dimethyl-N"-nitroguanidine | HCID 136218199 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Chloro-5-thiazolylmethyl)-3,3-dimethyl-l-methanesulphonyl-2-nitroguanidine | HCID 54283151 | 41.1% |
Reaction Steps
To a solution of 1-(2-chloro-5-thiazolylmethyl)-3,3- dimethyl-2-nitroguanidine (0.300 g) in an aqueous NaOH solution (NaOH (0.319 g) and water (10 ml)) were added CH2Cl2 (10 ml) and 4-dimethylaminopyridine (0.013 g). To the mixture was added methanesulphonyl chloride (0.391 g) dropwise at room temperature under stirring. After stirring for 30 minutes, the mixture was partitioned. The organic layer was dried over MgSO, and concentrated in vacuo. The resulting residue was applied to column chromatography on silica gel. The column was eluted with hexane-AcOEt (1:1) to afford 0.160 g of 1-(2-chloro-5-thiazolylmethyl)-3,3-dimethyl-l-methanesulphonyl-2-nitroguanidine (Compound No. 28) as a pale yellow crystal, m.p. 82°-86° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05256679 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-3af5a110d2d0447ab9064add5c3f9445 |
| Source note | uspto-grants-1993_10 |