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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119849Generated: October 31, 2026

(S)-(+)-4-(2,3-Epoxypropoxy)carbazole → (S)-4-[2-Hydroxy-3-([4-(4-hydroxyphenoxy)phenyl]-2-methylpropylamino)propoxy]carbazole

https://huagongshe.com/reaction/2119849

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-(+)-4-(2,3-Epoxypropoxy)carbazoleHCID 10879208—
Reactant4-(4-(2-Methyl-2-aminopropyl)phenoxy)phenolHCID 22147795—
SolventEthanolHCID 702—
Product(S)-4-[2-Hydroxy-3-([4-(4-hydroxyphenoxy)phenyl]-2-methylpropylamino)propoxy]carbazoleHCID 54318132—

Reaction Conditions

Temperature60 °C

Reaction Steps

4-(4-(2-Methyl-2-aminopropyl)phenoxy)phenol (0.40 g, 1.55 mmol) was combined with (S)-4-(oxiranylmethoxy)-9H-carbazole (0.250 g, 1.0 mmol) in EtOH (50 mL) and the mixture heated at 60° C. for 20 hours. The mixture was then concentrated in vacuo and the resulting residue chromatographed over silica (1-10% MeOH/CHCl3) which allowed for isolation of the product as the free base. The free base was then dissolved in minimal EtOAc and treated with diethyl ether (25 mL) saturated with HCl. Filtration and drying netted 0.410 g (76%) of product as the HCl salt. MS (FD+):497. m.p. 80-85° C. (dec). Anal. Calcd for C31H32N2O4.1.3HCl: C, 68.31; H, 6.16; N, 5.14. Found: C, 68.30; H, 6.75; N, 4.62.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686372B2
Source datasetuspto-grants-2004_02
ORD IDord-de2f22260768413e9ad9fc42f4537781
Source noteuspto-grants-2004_02