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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754196Generated: November 1, 2026

2-[(4-Quinolin-3-ylmethyl-piperazine-1-carbonyl)-amino]-benzoic acid methyl ester → 2-[(4-Quinolin-3-ylmethyl-piperazine-1-carbonyl)-amino]-benzoic acid

https://huagongshe.com/reaction/1754196

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[(4-Quinolin-3-ylmethyl-piperazine-1-carbonyl)-amino]-benzoic acid methyl esterHCID 11611120—
SolventTetrahydrofuranHCID 8028—
Product2-[(4-Quinolin-3-ylmethyl-piperazine-1-carbonyl)-amino]-benzoic acidHCID 57880880—

Reaction Steps

To a solution of 2-[(4-quinolin-3-ylmethyl-piperazine-1-carbonyl)-amino]-benzoic acid methyl ester (26 mg) in THF (0.5 mL) under N2 was added potassium trimethyl silanoate (9 mg) in one portion and the mixture was stirred at rt for 14 h. The mixture was concentrated to give the title compound as a white amorphous solid (22 mg). 1H NMR (400 MHz, CD3OD): 8.81 (d, J=2.1 Hz, 1H), 8.23-8.21 (m, 1H), 8.14 (dd, J=8.4, 0.9 Hz, 1H), 7.96-7.93 (m, 1H), 7.91 (dd, J=7.9, 1.6 Hz, 1H), 7.88-7.85 (m, 1H), 7.68 (ddd, J=8.4, 6.9, 1.4 Hz, 1H), 7.54 (ddd, J=8.1, 7.0, 1.1 Hz, 1H), 7.19-7.23 (m, 1H), 6.81-6.85 (m, 1H), 3.71 (s, 2H), 3.51-3.54 (m, 4H), 2.49-2.51 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169224B2
Source datasetuspto-grants-2015_10
ORD IDord-483c2d2759ed4a3f8aadb1dbd1a5df16
Source noteuspto-grants-2015_10