HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,5-Diazabicyclo(5,4,0)undec-5-ene → HCID 178465982, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,5-Diazabicyclo(5,4,0)undec-5-ene | HCID 314112 | — |
| Reactant | HCID 20077890 | HCID 20077890 | — |
| Reactant | HCID 178465983 | HCID 178465983 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178465982 | HCID 178465982 | 93.7% |
Reaction Steps
1.63 ml of 1,5-diazabicyclo(5.4.0)undec-5-ene followed by 3.15 g of N-(4-cyclopropyl-6-ethoxy-triazin-2-yl)-phenylcarbamate are added to a solution of 2.24 g of 3-difluoromethoxypyridin-2-yl-sulfonamide in 40 ml of acetonitrile. The reaction mixture is stirred for 45 minutes at room temperature and then concentrated using a rotary evaporator. The oily residue is triturated with 8 ml of 2N hydrochloric acid and diluted with 10 ml of water. The crystal mass is filtered off, washed with water and diethyl ether and dried, yielding 4.05 g of N-(3-difluoromethoxypyridine-2-sulfonyl)-N'-(4-cyclopropyl-6-ethoxy-triazin-2-yl)-urea having a melting point of 144°-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05407900 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-3b40538ff85442a1891425d87a0ce49a |
| Source note | uspto-grants-1995_04 |