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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015644Generated: October 30, 2026

HCID 16074975, compound → HCID 16074983, compound

https://huagongshe.com/reaction/1015644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 16074975HCID 16074975—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 16074983HCID 1607498318%

Reaction Steps

4-{[(2-Carboxy-5-phenyl-thiophen-3-yl)-(2,4-dichloro-benzoyl)-amino]-methyl}-piperidine-1-carboxylic acid benzyl ester (124 mg, 0.2 mmol) was dissolved in MeOH (2 mL) and treated with 10% Pd/C (200 mg) under H2 balloon. The reaction was stirred at room temperature for 18 h and the mixture was filtered on celite. The solution was evaporated to a residue that was purified by reverse-phase HPLC to provide 3-[(2,4-Dichloro-benzoyl)-piperidin-4-ylmethyl-amino]-5-phenyl-thiophene-2-carboxylic acid (17.3 mg, 18% yield). 1H NMR (CD3OD, 300 MHz): 7.55 (d, 1 H), 7.50 (m, 2 H), 7.27-7.39 (m, 4 H), 7.25 (s, 1 H), 7.18 (dd, 1 H), 4.12 (m, 1 H), 3.75 (m, 1 H), 3.43 (m, 2H), 2.96 (q, 2 H), 2.65 (d, 2 H), 2.05 (m, 1 H), 1.62 (m, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985769B2
Source datasetuspto-grants-2011_07
ORD IDord-97932f1fe7f1461b8c37a7fe731495c4
Source noteuspto-grants-2011_07