HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4-Benzo[4,5]furo[3,2-d]pyrimidin-4-yl-piperazine-1-carbothioic acid [4-(Pyrimidin-2-ylsulfamoyl)-phenyl]-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-(Piperazin-1-yl)benzofuro[3,2-d]pyrimidine | HCID 2368542 | — |
| Reactant | N-Pyrimidin-2-yl-4-thioformylamino-benzenesulfonamide chloride | HCID 86601004 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Benzo[4,5]furo[3,2-d]pyrimidin-4-yl-piperazine-1-carbothioic acid [4-(Pyrimidin-2-ylsulfamoyl)-phenyl]-amide | HCID 11753137 | — |
Reaction Steps
To a solution of 4-piperazinobenzofurano[3,2-d]pyrimidine (200 mg, 0.79 mmol) and pyridine (0.5 mL, 7.9 mmol) in dichloromethane (20 mL) was added a solution of product 1d in dichloromethane (20 mL) and this was stirred overnight. Methanol was added to quench excess thiophosgene; and the residue after removal of solvent was purified by silica gel column chromatography eluting with 5% methanol/dichloromethane and further recrystallized from dichloromethane/hexane to give 150 mg (37%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08999988B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-f51360050cf5415db699fdca2bd05cdb |
| Source note | uspto-grants-2015_04 |