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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265679Generated: October 30, 2026

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

https://huagongshe.com/reaction/1265679

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Amino-4-chloro-5-dimethylamino-phenyl)-carbamic acid tert.-butyl esterHCID 69688689—
Reactant(RS)-3-Oxo-3-{3-[5-(tetrahydro-pyran-2-yloxymethyl)-isoxazol-3-yl]-phenyl}-propionic acid tert.-butyl esterHCID 69689155—
Product(RS)-[4-Chloro-5-dimethylamino-2-(3-oxo-3-{3-[5-(tetrahydro-pyran-2-yloxymethyl)-isoxazol-3-yl]-phenyl}-propionylamino)-phenyl]-carbamic acid tert.-butyl esterHCID 86586836—

Reaction Steps

The title compound was prepared from (2-amino-4-chloro-5-dimethylamino-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 K15) according to the general procedure M. Obtained as a yellow foam (232 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544985B2
Source datasetuspto-grants-2003_04
ORD IDord-39ab58d74f2040f783deb3720efff386
Source noteuspto-grants-2003_04