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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266802Generated: November 1, 2026

tert-Butyl (2-amino-5-morpholino-4-(trifluoromethyl)phenyl)carbamate → (2-{3-[3-(5-Dimethylaminomethyl-[1,2,3]triazol-1-yl)-phenyl]-3-oxo-propionylamino}-5-morpholin-4-yl-4-trifluoromethyl-phenyl)-carbamic acid tert.-butyl ester

https://huagongshe.com/reaction/1266802

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (2-amino-5-morpholino-4-(trifluoromethyl)phenyl)carbamateHCID 12048026—
Reactant3-[3-(5-Dimethylaminomethyl-[1,2,3] triazol-1-yl)-phenyl]-3-oxo-propionic acid tert.-butyl esterHCID 69687667—
Product(2-{3-[3-(5-Dimethylaminomethyl-[1,2,3]triazol-1-yl)-phenyl]-3-oxo-propionylamino}-5-morpholin-4-yl-4-trifluoromethyl-phenyl)-carbamic acid tert.-butyl esterHCID 86586978—

Reaction Steps

The title compound was prepared from (2-amino-5-morpholin-4-yl-4-trifluoromethyl-phenyl)-carbamic acid tert.-butyl ester (Example J1) (181 mg, 0.5 mmol) and 3-[3-(5-dimethylaminomethyl-[1,2,3]triazol-1-yl)-phenyl]-3-oxo-propionic acid tert.-butyl ester (Example K8) (172 mg, 0.5 mmol) according to the general procedure M. Obtained as an amorphous yellow substance (179 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548495B2
Source datasetuspto-grants-2003_04
ORD IDord-e5cb921f99d3488b85fdb67c82695930
Source noteuspto-grants-2003_04