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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348613Generated: October 28, 2026

HCID 21072482, compound → HCID 21091492, compound

https://huagongshe.com/reaction/1348613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21072482HCID 21072482—
ReactantHCID 21091401HCID 21091401—
ReactantHCID 67077020HCID 67077020—
ProductHCID 21091492HCID 21091492—

Reaction Steps

((6R,7S)-9-Carbamoylmethyl-2-fluoro-6-methyl-8-oxo-6,7,8,9-tetrahydro-5-oxa-9-aza-benzocyclohepten-7-yl)-carbamic acid tert-butyl ester was deprotected according to the procedure in example 42b. The resulting 2-((6R,7S)-7-amino-2-fluoro-6-methyl-8-oxo-7,8-dihydro-6H-5-oxa-9-aza-benzocyclohepten-9-yl)-acetamide was reacted with 2,2-dimethyl-N-(2,2,3,3,3-pentafluoro-propyl)-malonamic acid in analogy to the procedure described in example 2b to yield N-((6R,7S)-9-carbamoylmethyl-2-fluoro-6-methyl-8-oxo-6,7,8,9-tetrahydro-5-oxa-9-aza-benzocyclohepten-7-yl)-2,2-dimethyl-N′-(2,2,3,3,3-pentafluoro-propyl)-malonamide, MS m/e (%): 511.3 (M−H+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211573B2
Source datasetuspto-grants-2007_05
ORD IDord-c162fb14e7964d65b3af6a179954de82
Source noteuspto-grants-2007_05