HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → 2-bromo-4,5,6,7-tetrahydro-N-(2-mercaptophenyl)-benzo[b]thiophene-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Bromo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylic acid | HCID 18422137 | — |
| Product | 2-bromo-4,5,6,7-tetrahydro-N-(2-mercaptophenyl)-benzo[b]thiophene-3-carboxamide | HCID 18422290 | — |
Reaction Steps
In the same manner as in Starting Material Synthesis Example 60 and using 2-bromo-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylic acid, thionyl chloride, 2-aminothiophenol, 2-bromo-4,5,6,7-tetrahydro-N-(2-mercaptophenyl)-benzo[b]thiophene-3-carboxamide is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06455521B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-2f79f879d0024c14a1151bd53d555063 |
| Source note | uspto-grants-2002_09 |