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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265677Generated: October 31, 2026

(2-Amino-5-dimethylamino-4-fluoro-phenyl)-carbamic acid tert.-butyl ester → (RS)-[5-Dimethylamino-4-fluoro-2-(3-oxo-3-{3-[3-(tetrahydro-pyran-2-yloxymethyl)-isoxazol-5-yl]-phenyl}-propionylamino)-phenyl]-carbamic acid tert.-butyl ester

https://huagongshe.com/reaction/1265677

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Amino-5-dimethylamino-4-fluoro-phenyl)-carbamic acid tert.-butyl esterHCID 69688174—
Reactant(RS)-3-oxo-3-{3-[3-(tetrahydro-pyran-2-yloxymethyl)-isoxazol-5-yl]-phenyl}-propionic acid tert.-butyl esterHCID 69688926—
Product(RS)-[5-Dimethylamino-4-fluoro-2-(3-oxo-3-{3-[3-(tetrahydro-pyran-2-yloxymethyl)-isoxazol-5-yl]-phenyl}-propionylamino)-phenyl]-carbamic acid tert.-butyl esterHCID 86586834—

Reaction Steps

The title compound was prepared from (2-amino-5-dimethylamino-4-fluoro-phenyl)-carbamic acid tert.-butyl ester (Example J13) (269 mg, 1.0 mmol) and (RS)-3-oxo-3-{3-[3-(tetrahydro-pyran-2-yloxymethyl)-isoxazol-5-yl]-phenyl}-propionic acid tert.-butyl ester (Example K12) (401 mg, 1.0 mmol) according to the general procedure M. Obtained as a yellow amorphous substance (360 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544985B2
Source datasetuspto-grants-2003_04
ORD IDord-d862f3510717428b97bb6bb31606ee83
Source noteuspto-grants-2003_04