HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyltetrahydrofuran → HCID 131735051, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(2-(Trifluoromethyl)pyridin-4-ylamino)cyclopent-2-enone | HCID 90311002 | — |
| Reactant | Tert-butyl(4-cyanophenyl)(phenylsulfonyl)methylcarbamate | HCID 129539717 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131735051 | HCID 131735051 | — |
Reaction Steps
Sodium hydride (60% in mineral oil, 895 mg, 22.4 mmol) is added in portions to a mixture of 3-(2-(trifluoromethyl)pyridin-4-ylamino)cyclopent-2-enone (intermediate 17, 4.52 g, 18.7 mmol) and 2-methyltetrahydrofuran (30 mL). After 30 min tert-butyl (4-cyano-phenyl)(phenylsulfonyl)methylcarbamate (6.90 g, 18.5 mmol) is added, and mixture is stirred at room temperature for 30 min Water is added, and the phases are separated. The organic phase is dried over Na2SO4 and concentrated under reduced pressure. Yield: 9.20 g; ESI mass spectrum [M+H]+=473; Retention time HPLC: 1.09 min (Z018_504).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290459B1 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-79998569317144fbb002cf92b9119a60 |
| Source note | uspto-grants-2016_03 |