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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242496Generated: October 31, 2026

Methyl 3-Hydroxyphenylacetate → HCID 69666999, compound

https://huagongshe.com/reaction/1242496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-HydroxyphenylacetateHCID 39129—
Reactanttert-Butyl 2-bromo-2-methylpropionateHCID 90290—
Reactant3-(1-tert-Butoxycarbonyl-1-methylethoxy)phenylacetic AcidHCID 18766414—
Reactant4-Trifluoromethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acidHCID 21935767—
ReactantHCID 21935904HCID 21935904—
ProductHCID 69666999HCID 69666999—

Reaction Steps

In analogy to the procedures described in example 26B] and 124C], 4-cyclopropyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-ylamine (prepared from 4-trifluoromethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acid, see example 133], in analogy to the procedures described in examples 125B] and 125C]) was reacted with 2-(3-carboxymethyl-phenoxy)-2-methyl-propionic acid tert-butyl ester (prepared from (3-hydroxy-phenyl)-acetic acid methyl ester and tert-butyl alpha-bromoisobutyrate, in analogy to the procedure described in example 52A], followed by saponification in analogy the procedure described in example 124A]) to give 2-(3-{[4-cyclopropyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-ylcarbamoyl]-methyl}-phenoxy)-2-methyl-propionic acid tert-butyl ester, which was subsequently cleaved with trifluoroacetic acid to yield the title compound as light yellow amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115611B2
Source datasetuspto-grants-2006_10
ORD IDord-4eda39b34a3149bd8d93f340143fa7df
Source noteuspto-grants-2006_10