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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509773Generated: October 31, 2026

Tert-butyl 2-((pyridin-2-ylmethyl)(4-sulfamoylphenethyl)amino)acetate → 2-((Pyridin-2-ylmethyl)(4-sulfamoylphenethyl)amino)acetic acid

https://huagongshe.com/reaction/1509773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 2-((pyridin-2-ylmethyl)(4-sulfamoylphenethyl)amino)acetateHCID 46233926—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
Product2-((Pyridin-2-ylmethyl)(4-sulfamoylphenethyl)amino)acetic acidHCID 44156947100%

Reaction Steps

To a solution of tert-butyl 2-((pyridin-2-ylmethyl)(4-sulfamoylphenethyl)amino)acetate (150 mg, 0.37 mmol) in DCM (3.0 mL) and TFA (3.0 mL) was stirred at room temperature for overnight. The solvent was removed under reduced pressure to give 2-((pyridin-2-ylmethyl)(4-sulfamoylphenethyl)amino)acetic acid (129 mg, 100%). 1H NMR (400 MHz, CD3OD) δ 8.73 (d, J=5.6 Hz, 0.46 H), 8.58 (d, J=4.4 Hz, 1H), 8.57 (t, J=8.0 Hz, 0.46H), 8.16 (t, J=7.6 Hz, 1H), 8.01 (d, J=8.4 Hz, 0.54 H), 7.96 (t, J=6.8 Hz, 0.54H), 7.79 (d, J=8.4 Hz, 2H), 7.66 (d, J=7.2 Hz, 2H), 7.35 (d, J=8.4 Hz, 2H), 4.51 (s, 2H), 4.06 (s, 2H), 3.36 (t, J=7.6 Hz, 2H), 3.05 (t, J=7.6 Hz, 2H); ESMS m/z: 355 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211402B2
Source datasetuspto-grants-2012_07
ORD IDord-2abff68427a14542829dca56fb457ba4
Source noteuspto-grants-2012_07