HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophosgene → HCID 20192957, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | HCID 20192941 | HCID 20192941 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 20192957 | HCID 20192957 | — |
Reaction Steps
To a cooled mixture of 1.5 g of 6-amino-2-tert-butyl-5-[3-methylpiperidin-1-yl]benzothiazole and 1.5 g of potassium bicarbonate in 50 ml of chloroform is added dropwise 0.6 g of thiophosgene in 5 ml of chloroform under stirring. The stirring is continued for 30 minutes maintaining the temperature at 0°-2°. The solid is filtered and the filtrate is evaporated. The residue thus obtained is dissolved in chloroform and filtered through a silica gel column. The filtrate is evaporated to give 2-tert-butyl-6-isothiocyanato-5-[3-methylpiperidin-1-yl]benzothiazole, melting at 47°-52°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04680301 |
| Source dataset | uspto-grants-1987_07 |
| ORD ID | ord-4cc25fd801834f62baca4f8c88d544bc |
| Source note | uspto-grants-1987_07 |