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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179338Generated: October 31, 2026

tert-Butyl (2-{2-[(4-{[(benzylamino)carbonyl]amino}benzyl)-amino]-2-oxoethyl}-1-oxo-2,3,4,5-tetrahydro-1H-2-benzazepin-5-yl)acetate → (2-{2-[(4-{[(Benzylamino)carbonyl]amino}benzyl)amino]-2-oxoethyl}-1-oxo-2,3,4,5-tetrahydro-1H-2-benzazepin-5-yl)acetic Acid

https://huagongshe.com/reaction/1179338

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (2-{2-[(4-{[(benzylamino)carbonyl]amino}benzyl)-amino]-2-oxoethyl}-1-oxo-2,3,4,5-tetrahydro-1H-2-benzazepin-5-yl)acetateHCID 86591657—
SolventTrifluoroacetic acidHCID 6422—
Product(2-{2-[(4-{[(Benzylamino)carbonyl]amino}benzyl)amino]-2-oxoethyl}-1-oxo-2,3,4,5-tetrahydro-1H-2-benzazepin-5-yl)acetic AcidHCID 69429177—

Reaction Conditions

Temperature0 °C

Reaction Steps

40 mg (0.07 mmol) of Example III are dissolved in 3 ml of trifluoroacetic acid and the mixture is stirred at 0° C. for 2 h and at room temp. for 16 h. It is concentrated, and the residue is codistilled repeatedly with CH2Cl2 and dried (31.8 mg). ESI-MS [M+H+]=515.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279468B2
Source datasetuspto-grants-2007_10
ORD IDord-fb8bc812493141fcbea7d845ac1f864b
Source noteuspto-grants-2007_10