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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348658Generated: October 31, 2026

2-Hydroxy-2-methyl-N-(3,3,3-trifluoro-propyl)-malonamic acid → HCID 131726361, compound

https://huagongshe.com/reaction/1348658

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Hydroxy-2-methyl-N-(3,3,3-trifluoro-propyl)-malonamic acidHCID 21091409—
ReactantHCID 21091439HCID 21091439—
ProductHCID 131726361HCID 131726361—

Reaction Steps

N-[(6R,7S)-2-Fluoro-6-methyl-8-oxo-9-(2,2,2-trifluoro-ethyl)-6,7,8,9-tetrahydro-5-oxa-9-aza-benzocyclohepten-7-yl]-2-(R or S)-hydroxy-2-methyl-N′-(3,3,3-trifluoro-propyl)-malonamide was obtained as mixture of epimers according to the procedures described for example 2b using racemic 2-hydroxy-2-methyl-N-(3,3,3-trifluoro-propyl)-malonamic acid and (6R,7S)-7-amino-2-fluoro-6-methyl-9-(2,2,2-trifluoro-ethyl)-6,7-dihydro-9H-5-oxa-9-aza-benzocyclohepten-8-one. The epimers were separated by chromatography on Chiralpak AD using ethanol/heptane 15:85 to yield (−)-N-[(6R,7S)-2-fluoro-6-methyl-8-oxo-9-(2,2,2-trifluoro-ethyl)-6,7,8,9-tetrahydro-5-oxa-9-aza-benzocyclohepten-7-yl]-2-(R or S)-hydroxy-2-methyl-N′-(3,3,3-trifluoro-propyl)-malonamide, entity A, MS m/e (%): 504.0 (M+H+, 100), as first eluting fraction, and (−)-N-[(6R,7S)-2-fluoro-6-methyl-8-oxo-9-(2,2,2-trifluoro-ethyl)-6,7,8,9-tetrahydro-5-oxa-9-aza-benzocyclohepten-7-yl]-2-(R or S)-hydroxy-2-methyl-N′-(3,3,3-trifluoro-propyl)-malonamide, entity B, as second eluting fraction, MS m/e (%): 504.0 (M+H+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211573B2
Source datasetuspto-grants-2007_05
ORD IDord-57b8c6b2f32c403fb939358780bf9220
Source noteuspto-grants-2007_05