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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615244Generated: October 26, 2026

2-((4-(2-(Cyclopropylmethoxy)ethyl)phenoxy)methyl)oxirane → 1-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-ethyl]-benzylamino]-3-[4-[2-(cyclopropylmethoxy)ethyl]-phenoxy]-2-propanol

https://huagongshe.com/reaction/615244

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-((4-(2-(Cyclopropylmethoxy)ethyl)phenoxy)methyl)oxiraneHCID 11791542—
Reactant5-(2-Benzylaminopropoxy)salicylamideHCID 13754334—
SolventIsopropanolHCID 3776—
Product1-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-ethyl]-benzylamino]-3-[4-[2-(cyclopropylmethoxy)ethyl]-phenoxy]-2-propanolHCID 20151321—

Reaction Steps

A solution of 14.3 g of 1-[2-(cyclopropyl-methoxy)-ethyl]-4-(2,3-epoxypropoxy)-benzene (German Offenlegungsschrift No. 2,649,605) and 16.3 g of 5-[2-(benzylamino)-propoxy]-salicylamide in 200 ml of isopropanol is refluxed for 18 hours. The reaction mixture is concentrated by evaporation to leave crude 1-[N-[2-(3-carbamoyl-4-hydroxyphenoxy)-ethyl]-benzylamino]-3-[4-[2-(cyclopropylmethoxy)-ethyl]-phenoxy]-2-propanol in the form of brown oil, which can be further processed without additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04497813
Source datasetuspto-grants-1985_02
ORD IDord-c7e4511312f344bdb523e33a6262229f
Source noteuspto-grants-1985_02