HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chloro-N-((S)-2,3-dihydroxypropyl)thiophene-2-carboxamide → 5-Chloro-N-((2R)-2-hydroxy-3-((4-(3-oxo-4-morpholinyl)phenyl)amino)propyl)-2-thiophenecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chloro-N-((S)-2,3-dihydroxypropyl)thiophene-2-carboxamide | HCID 9991690 | — |
| Reactant | N-((S)-3-bromo-2-hydroxypropyl)-5-chlorothiophene-2-carboxamide | HCID 10108741 | — |
| Reactant | 4-(4-Aminophenyl)morpholin-3-one | HCID 11194854 | — |
| Product | 5-Chloro-N-((2R)-2-hydroxy-3-((4-(3-oxo-4-morpholinyl)phenyl)amino)propyl)-2-thiophenecarboxamide | HCID 10001574 | — |
Reaction Steps
In this case, 5-chlorothiophene-2-carbonyl chloride (IV) is reacted with (28)-3-aminopropane-1,2-diol hydrochloride (VII) to give 5-chlorothiophene-2-carboxylic acid ((S)-2,3-dihydroxypropyl)-amide (IX). Subsequently, (IX) is converted into 5-chlorothiophene-2-carboxylic acid ((S)-3-bromo-2-hydroxypropyl)amide (X), which is then reacted with 4-(4-aminophenyl)-3-morpholinone (III) to give 5-chlorothiophene-2-carboxylic acid {(R)-2-hydroxy-3-[4-(3-oxomorpholin-4-yl)phenylamino]-propyl}amide (XI). Finally, (XI) is reacted with phosgene or a phosgene equivalent to give 5-chloro-N-({(5S)-2-oxo-3-[4-(3-oxo-4-morpholinyl)phenyl]-1,3-oxazolidin-5-yl}methyl)-2-thiophenecarboxamide (I).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351823B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-159151f55feb40e6ac45b3ce4c151abb |
| Source note | uspto-grants-2008_04 |