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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266807Generated: November 2, 2026

tert-Butyl (2-amino-5-morpholino-4-(trifluoromethyl)phenyl)carbamate → (RS)-[5-Morpholin-4-yl-2-(3-oxo-3-{3-[5-(tetrahydro-pyran-2-yloxymethyl)-isoxazol-3-yl]-phenyl}-propionylamino)-4-trifluoromethyl-phenyl]-carbamic acid tert.-butyl ester

https://huagongshe.com/reaction/1266807

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (2-amino-5-morpholino-4-(trifluoromethyl)phenyl)carbamateHCID 12048026—
Reactant(RS)-3-Oxo-3-{3-[5-(tetrahydro-pyran-2-yloxymethyl)-isoxazol-3-yl]-phenyl}-propionic acid tert.-butyl esterHCID 69689155—
Product(RS)-[5-Morpholin-4-yl-2-(3-oxo-3-{3-[5-(tetrahydro-pyran-2-yloxymethyl)-isoxazol-3-yl]-phenyl}-propionylamino)-4-trifluoromethyl-phenyl]-carbamic acid tert.-butyl esterHCID 86586983—

Reaction Steps

The title compound was prepared from (2-amino-5-morpholin-4-yl-4-trifluoromethyl-phenyl)-carbamic acid tert.-butyl ester (Example J1) and (RS)-3-oxo-3-{3-[5-(tetrahydro-pyran-2-yloxymethyl)-isoxazol-3-yl]-phenyl}-propionic acid tert.-butyl ester (Example K11) according to the general procedure M. Obtained as a light yellow foam (774 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548495B2
Source datasetuspto-grants-2003_04
ORD IDord-4b07d63998184acca0b813891df72958
Source noteuspto-grants-2003_04