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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787061Generated: October 31, 2026

3-Chloro-4-[3-(trifluoromethyl)phenoxy]aniline → HCID 67520502, compound

https://huagongshe.com/reaction/1787061

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-[3-(trifluoromethyl)phenoxy]anilineHCID 19626984—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
ReactantHCID 57597274HCID 57597274—
ReactantHCID 86615791HCID 86615791—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
ProductHCID 67520502HCID 67520502—

Reaction Steps

3-{2-[4-({3-Chloro-4-[3-(trifluoromethyl)phenoxy]phenyl}amino)-5H-pyrrolo[3,2-d]pyrimidin-5-yl]ethoxy}propane-1,2-diol was obtained by the reaction in the same manner as in Example 237 (iv) using 4-chloro-5-{2-[(2,2-dimethyl-1,3-dioxolan-4-yl)methoxy]ethyl}-5H-pyrrolo[3,2-d]pyrimidine (295 mg), 3-chloro-4-[3-(trifluoromethyl)phenoxy]aniline (359 mg) and isopropyl alcohol (6 mL). The obtained 3-{2-[4-({3-chloro-4-[3-(trifluoromethyl)phenoxy]phenyl}amino)-5H-pyrrolo[3,2-d]pyrimidin-5-yl]ethoxy}propane-1,2-diol was dissolved in ethyl acetate (6 mL), 4N hydrochloric acid-ethyl acetate (0.2 mL) was added, and the mixture was concentrated under reduced pressure. The residue was crystallized from ethyl acetate to give the title compound (360 mg) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507740B2
Source datasetuspto-grants-2009_03
ORD IDord-66ccf0905d1247ef9bb07dee9ad0924b
Source noteuspto-grants-2009_03