HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Cyano-3,3-bis(methylthio)acrylamide → 2-Cyano-3-[[(3S)-hexahydro-2-oxo-1-(phenylmethyl)-1H-azepin-3-yl]amino]-3-[(2-methyl-5-benzofuranyl)amino]-propenamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Cyano-3,3-bis(methylthio)acrylamide | HCID 2747746 | — |
| Reactant | 2-Methyl-5-benzofuranamine | HCID 3157484 | — |
| Reactant | 3-Amino-1-benzyl-azepan-2-one | HCID 18612599 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Cyano-3-[[(3S)-hexahydro-2-oxo-1-(phenylmethyl)-1H-azepin-3-yl]amino]-3-[(2-methyl-5-benzofuranyl)amino]-propenamide | HCID 70032036 | 37% |
Reaction Steps
Preparation of title compound. A solution of 2-methyl-5-benzofuranamine (32 mg, 0.22 mmol) and 3,3-bis(methylthio)-2-cyanoacrylamide (41 mg, 0.22 mmol) in ethanol (0.35 mL) was stirred at 80° C. After stirring for 5 h, a solution of 3-aminohexahydro-1-phenylmethyl-2H-azepin-2-one (74 mg, 0.29 mmol) in ethanol (0.74 mL) was added. After stirring at 80° C. for 2 days, the reaction was purified by column chromatography (silica, 1% methanol/dichloromethane) to afford the title compound (37 mg, 37% yield): MS (ESI, pos. ion spectrum) m/z 458; HPLC (method A) tR 4.13 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06544981B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-44dae7d193bc481b8840d58d8d9c28f4 |
| Source note | uspto-grants-2003_04 |