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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921430Generated: October 31, 2026

Piperidin-3-ylmethanol → HCID 58808752, compound

https://huagongshe.com/reaction/1921430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidin-3-ylmethanolHCID 107308—
Reactant5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-sulfonyl chlorideHCID 86610352—
ProductHCID 58808752HCID 5880875254.7%

Reaction Steps

5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-sulfonyl chloride is reacted with 3-hydroxymethylpiperidine as described in Step 5, Example 24 to give the title compound as a solid (54.7% yield). LC/MS: RT 2.63 min; m/e 397 (M+H); 1H NMR (δ, ppm): 11.8 (1H, s), 7.6 (1H, d); 7.4 (1H, s); 7.24 (1H, d), 4.6 (1H, br s), 3.6 (21H, m), 3.2 (1H, m), 2.4 (2H, q), 2.36 (3H, s), 2.1 (1H, t), 1.8-1.4 (5H, m), 1.1 (3H, t), 0.94 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173682B2
Source datasetuspto-grants-2012_05
ORD IDord-2cfe73b29eaf40cb8efb1c719f194a50
Source noteuspto-grants-2012_05