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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242491Generated: October 26, 2026

(S)-N-(3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl)-5-methyl-3-(2,4,5-trifluorophenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine-1-carboxamide → HCID 46862780, compound

https://huagongshe.com/reaction/242491

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-N-(3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl)-5-methyl-3-(2,4,5-trifluorophenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine-1-carboxamideHCID 46863441—
Reactant(S)-2-amino-N-(2-hydroxyethyl)-3,3-dimethylbutanamideHCID 58124726—
Reactanttert-butyl 3-(5-chloro-2-fluorophenyl)-6,7-dihydro-1H-pyrazolo[4,3-b]pyridine-4(5H)-carboxylateHCID 59345330—
ProductHCID 46862780HCID 46862780—

Reaction Steps

Compound 94 was prepared according to the procedure for the synthesis of compound 37 by replacing intermediate 19 with intermediate 20D, and replacing tert-leucine methylamide with intermediate 23. LCMS (+ESI) m/z=466.3 [M+H]+. 1H NMR (CDCl3) δ 7.80 (d, J=8.9 Hz, 1H), 7.62-7.65 (m, 1H), 7.32-7.37 (m, 1H), 7.10 (t, J=9.0 Hz, 1H), 4.14 (d, J=8.9 Hz, 1H), 3.71 (br, 2H), 3.42-3.46 (m, 2H), 3.02-3.06 (m, 2H), 2.96 (br, 2H), 2.41 (s, 3H), 1.92 (br, 2H), 1.06 (s, 9H). Purity: 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653127B2
Source datasetuspto-grants-2014_02
ORD IDord-38290ccf474341a394c22d33499cfb1e
Source noteuspto-grants-2014_02