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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638035Generated: October 29, 2026

Methyl iodide → HCID 20255167, compound

https://huagongshe.com/reaction/638035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178513693HCID 178513693—
SolventDimethylformamideHCID 6228—
ProductHCID 20255167HCID 20255167—

Reaction Steps

At 0°, 0.18 g of potassium tert.-butoxide is added to a solution of 1.0 g of 1-[N-benzyl-2-(3-carbamoyl-4-benzyloxyphenoxy)-ethylamino]-3-[4-[4-(trifluoromethyl)-1H-imidazol-2-yl]-phenoxy]-2-propanol in 5 ml of dimethylformamide and the mixture is stirred for 20 minutes in an ice bath. At 0°-5°, a solution of 0.12 ml of methyl iodide in 3 ml of dimethylformamide is added and the mixture is then stirred for 4 hours at room temperature. The reaction solution is concentrated by evaporation, the residue is dissolved in water and the solution is extracted with ethyl acetate. After drying the organic phase over sodium sulphate, this is concentrated to dryness by evaporation, yielding the crude 1-[N-benzyl-2-(3-carbamoyl-4-benzyloxyphenoxy)-ethylamino]-3-[4-[1-methyl-4-(trifluoromethyl)-1H-imidazol-2-yl]-phenoxy]-2-propanol which is further processed in that form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04559354
Source datasetuspto-grants-1985_12
ORD IDord-c3aaab5e4d324943b814f6571d72483c
Source noteuspto-grants-1985_12