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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545185Generated: October 29, 2026

6-(1-methyl-1H-pyrazol-4-yl)spiro[chroman-2,4'-piperidin]-4-one → HCID 178488445, compound

https://huagongshe.com/reaction/545185

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(1-methyl-1H-pyrazol-4-yl)spiro[chroman-2,4'-piperidin]-4-oneHCID 57519244—
ReactantHCID 178488446HCID 178488446—
ProductHCID 178488445HCID 178488445—

Reaction Steps

The compound is synthesized according to the procedure described in Example 1, using 6-(1-methyl-1H-pyrazol-4-yl)spiro[chroman-2,4′-piperidin]-4-one instead of 4-oxospiro(chroman-2,4′-piperidin)-6-yl acetamide, and 8-methoxy-4-(1H-tetrazol-5-yl)-2-naphthoic acid instead of 4,8-dimethoxyquinoline-2-carboxylic acid. 1H-NMR (400 MHz, DMSO-d6) δ: 8.39 (1H, s), 8.21 (1H, d, J=8.0 Hz), 8.12 (1H, s), 8.01 (1H, d, J=2.0 Hz), 7.83-7.77 (3H, m), 7.63 (1H, t, J=8 Hz), 7.15 (1H, d, J=8 Hz), 7.11 (1H, d, J=8.0 Hz), 4.40-4.22 (1H, m), 4.02 (3H, s), 3.83 (3H, s), 3.70-3.30 (3H, m), 2.89 (2H, s), 2.12-1.75 (4H, m). MS [M+H]+=550.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935712B2
Source datasetuspto-grants-2011_05
ORD IDord-285e9347d1564f29b38c948558c701cb
Source noteuspto-grants-2011_05