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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921421Generated: October 28, 2026

1-(Cyclopropylmethyl)piperidin-4-amine → 5-[5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl]thiophene-2-sulfonic acid (1-cyclopropylmethylpiperidin-4-yl)amide hydrochloride

https://huagongshe.com/reaction/1921421

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Cyclopropylmethyl)piperidin-4-amineHCID 17221624—
Reactant5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-sulfonyl chlorideHCID 86610352—
Product5-[5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl]thiophene-2-sulfonic acid (1-cyclopropylmethylpiperidin-4-yl)amide hydrochlorideHCID 1169851458%

Reaction Steps

5-(5-Ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)thiophene-2-sulfonyl chloride is reacted with (1-cyclopropylmethylpiperidin-4-yl)amine as described in Steps 5 and 6, Example 24 to give the title compound as a white solid (58% yield). LC/MS: RT 2.07 min; m/e 436; 1H NMR (δ, ppm): 11.85 (1H, br), 10.18 (1H, br), 8.30 (1H, d), 7.57 (1H, d), 7.34 (1H, s), 7.17 (1H, d), 3.30-3.58 (2H, m), 2.80-3.08 (2H, m), 2.40 (2H, q), 2.33 (3H, s), 1.72-2.18 (4H, m), 1.00-1.20 (4H, m), 0.60 (2H, m), 0.35 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173682B2
Source datasetuspto-grants-2012_05
ORD IDord-0d5db943693a44ad8e5a26660b879428
Source noteuspto-grants-2012_05