HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 3-Chloromethyl-5,6-dimethoxy-1-(1-trityl-4-imidazolyl)methyl-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5,6-dimethoxy-1-(1-trityl-4-imidazolyl)methyl-1H-indazole-3-methanol | HCID 15428638 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Chloromethyl-5,6-dimethoxy-1-(1-trityl-4-imidazolyl)methyl-1H-indazole | HCID 15428639 | — |
Reaction Steps
5,6-Dimethoxy-1(1-trityl-4-imidazolyl)methyl-1H -indazole-3-methanol (180.0 g), which had been ground in a mortar, was suspended in dichloromethane (1700 ml) at room temperature and then cooled with ice/water. Next, thionyl chloride (48.6 ml) was dropped thereinto within 5 minutes. The reaction mixture was poured into a saturated aqueous solution of sodium bicarbonate (2000 ml) and extracted with chloroform (5000 ml). After drying over sodium sulfate, filtering and evaporating under reduced pressure, a colorless solid was obtained (165.1 g). This solid product was used in the subsequent reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05661150 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-7f513d419ab44e8b803173fa8555b14d |
| Source note | uspto-grants-1997_08 |