HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242496Generated: October 31, 2026
Methyl 3-Hydroxyphenylacetate → HCID 69666999, compound
https://huagongshe.com/reaction/1242496
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 3-Hydroxyphenylacetate | HCID 39129 | — |
| Reactant | tert-Butyl 2-bromo-2-methylpropionate | HCID 90290 | — |
| Reactant | 3-(1-tert-Butoxycarbonyl-1-methylethoxy)phenylacetic Acid | HCID 18766414 | — |
| Reactant | 4-Trifluoromethyl-2-(4-trifluoromethyl-phenyl)-pyrimidine-5-carboxylic acid | HCID 21935767 | — |
| Reactant | HCID 21935904 | HCID 21935904 | — |
| Product | HCID 69666999 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115611B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-4eda39b34a3149bd8d93f340143fa7df |
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| Source note | uspto-grants-2006_10 |
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