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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519321Generated: October 31, 2026

3-Methoxybenzylamine → HCID 71538330, compound

https://huagongshe.com/reaction/1519321

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxybenzylamineHCID 21156—
ReactantHCID 86679835HCID 86679835—
ProductHCID 71538330HCID 7153833077%

Reaction Steps

Using the conditions of General Procedure E for Amide Coupling in Parallel Mode, 4-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-biphenyl-2,4′-dicarboxylic acid 2-methyl ester (which may be prepared as described for Intermediate 8; 100 mg, 0.21 mmol) was reacted with 3-methoxybenzylamine (available from Aldrich Chemical Company, Inc.; 85 mg, 0.62 mmol). The resulting ester was hydrolyzed and the acid was purified using HPLC Purification Conditions B to give 4-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-4′-(3-methoxy-benzylcarbamoyl)-biphenyl-2-carboxylic acid (94 mg, 77%). 1H NMR (400 MHz, DMSO-d6) δ ppm 13.18 (br s, 1H), 9.08 (t, J=5.6 Hz, 1H), 8.46 (s, 1H), 8.38 (s, 1H), 8.33 (s, 1H), 8.24 (d, J=8.0 Hz, 1H), 8.09 (d, J=8.5 Hz, 1H), 7.96 (d, J=7.8 Hz, 2H), 7.76 (d, J=8.3 Hz, 1H), 7.59 (d, J=8.0 Hz, 1H), 7.50 (d, J=7.8 Hz, 2H), 7.26 (t, J=7.9 Hz, 1H), 6.89-6.94 (m, 2H), 6.83 (d, J=8.3 Hz, 1H), 4.49 (d, J=5.8 Hz, 2H), 3.75 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073881B2
Source datasetuspto-grants-2015_07
ORD IDord-19677d491b5a400fbaaabf51d66b22d1
Source noteuspto-grants-2015_07