HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoroethyl bromide → N1,N1-dimethyl-N2-([4-(2-fluoroethoxy)-2-methyl-2H-indazol-3-yl]sulfonyl}formamidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoroethyl bromide | HCID 12982 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 136000308 | HCID 136000308 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N1,N1-dimethyl-N2-([4-(2-fluoroethoxy)-2-methyl-2H-indazol-3-yl]sulfonyl}formamidine | HCID 86749619 | 69.5% |
Reaction Steps
4.2 g (15 mmol) of N1,N1 -dimethyl-N2 -[(4-hydroxy-2-methyl-2H-indazol-3-yl)sulfonyl]formamidine was added to a suspension containing 0.6 g (15 mmol) of 60% sodium hydride in 50 ml of DMF, and the mixture was stirred at room temperature for one hour. Further, 2 g (16 mmol) of 1-bromo-2-fluoroethane was added thereto, and the mixture was stirred at room temperature for 12 hours. The mixture was poured into ice water, and the formed crystals were collected by filtration and washed with water and IPE to obtain the desired product. This product was used for the subsequent reaction without purification. Obtained amount: 3.4 g (yield: 69.5%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05670452 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-3955f944978b4834917b6383f4f7562f |
| Source note | uspto-grants-1997_09 |