HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 4-amino-N-(5-benzyl[1.3.4]thiadiazol-2-yl)-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-butyl [4-(5-benzyl[1.3.4]thiadiazol-2-ylcarbamoyl)phenyl]carbamate | HCID 86662112 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-amino-N-(5-benzyl[1.3.4]thiadiazol-2-yl)-benzamide | HCID 66739948 | 92.1% |
Reaction Steps
0.2 g of tert-butyl [4-(5-benzyl[1.3.4]thiadiazol-2-ylcarbamoyl)phenyl]carbamate (0.49 mmol, 1 eq.) is placed in 5 mL of dichloromethane. 1 mL of trifluoroacetic acid (13.54 mmol, 27.6 eq.) is added and the reaction medium is stirred for 3 days at room temperature. The solvents are evaporated off and the residue is taken up in diethyl ether and pentane to give 0.14 g of 4-amino-N-(5-benzyl[1.3.4]thiadiazol-2-yl)-benzamide acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546391B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-d4284ddb46264b769d984419f915c718 |
| Source note | uspto-grants-2013_10 |