HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Chloro-N-(3-{[3-fluoro-4-(3-oxo-4-morpholinyl)phenyl]amino}-2-hydroxypropyl)-2-thiophenecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 5-chloro-N-(2-oxiranylmethyl)-2-thiophenecarboxamide | HCID 21919798 | — |
| Reactant | 4-(4-Amino-2-fluoro-phenyl)-morpholin-3-one | HCID 23105311 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Chloro-N-(3-{[3-fluoro-4-(3-oxo-4-morpholinyl)phenyl]amino}-2-hydroxypropyl)-2-thiophenecarboxamide | HCID 21070710 | — |
Reaction Steps
800 mg (3.8 mmol) of 4-(4-amino-2-fluorophenyl)-3-morpholinone and 700 mg (3.22 mmol) of 5-chloro-N-(2-oxiranylmethyl)-2-thiophenecarboxamide are heated in 15 ml of ethanol and 1 ml of water under reflux for 6 hours. The mixture is evaporated in vacuo, the crystals which have separated out after treatment with ethyl acetate are filtered off with suction, and chromatography of the mother liquor results in 276 mg (17% of theory) of the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07767702B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-23c0b1ef7eef4a439f61e36f51cb7ac1 |
| Source note | uspto-grants-2010_08 |