Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58469Generated: October 30, 2026

Cyclopropanecarboxaldehyde → HCID 118483449, compound

https://huagongshe.com/reaction/58469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarboxaldehydeHCID 123114—
Reactant(4-(3-Fluoro-2-(trifluoromethyl)phenyl)piperidin-1-yl)(4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridin-3-yl)methanone HydrochlorideHCID 118483339—
ReactantHCID 118483518HCID 118483518—
ProductHCID 118483449HCID 118483449—

Reaction Steps

Following general procedure GP-G1, ((4-(3-fluoro-2-(trifluoro-methyl)phenyl)piperidin-1-yl)(4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridin-3-yl)methanone hydrochloride (30) and cyclopropane carbaldehyde were converted to (6-ethyl-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridin-3-yl)(4-(3-fluoro-2-(trifluormethyl)phenyl) piperidin-1-yl)methanone as a white solid (23 mg, 34%): 1H NMR (300 MHz, DMSO-d6) δ 12.74 (br s, 1H), 7.72-7.65 (m, 1H), 7.47 (d, J=7.8 Hz, 1H), 7.34-7.27 (m, 1H), 4.92-4.63 (m, 2H), 3.59-3.53 (m, 2H), 3.32-3.09 (m, 2H), 2.90-2.39 (m, 7H), 1.81-1.62 (m, 4H), 0.92-0.85 (m, 1H), 0.52-0.48 (m, 2H), 0.14-0.10 (m, 2H); ESI MS m/z 451 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434727B2
Source datasetuspto-grants-2016_09
ORD IDord-aa2e72c91a544f47ae5e3580a12a78e6
Source noteuspto-grants-2016_09