Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649924Generated: November 1, 2026

Trityl chloride → amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptane

https://huagongshe.com/reaction/1649924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
ReactantHCID 178484877HCID 178484877—
SolventDichloromethaneHCID 6344—
Productamino-1-cyclohexyl-3(S)-hydroxy-6-methylheptaneHCID 57008919270.1%

Reaction Steps

To a solution of 2(S)-(Nα -methyl-L-histidyl)amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptane (900 mg) and triethylamine (494 mg) in methylene chloride (20 ml) was added trityl chloride (696 mg) at 0° C. The mixture was stirred at the same temperature for 1 hour. After evaporation of the solvent, the residue was dissolved in ethyl acetate (30 ml) and the solution was washed with 1M sodium bicarbonate solution and water successively, and dried over magnesium.sulfate. Evaporation of the solvent gave 2(S)-(Nα -methyl-Nim -trityl-L-histidyl)amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptane (1.46 g) as an amorphous powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04921855
Source datasetuspto-grants-1990_05
ORD IDord-6cef93508e844c3099ee7e1e90a3b07e
Source noteuspto-grants-1990_05