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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982502Generated: October 28, 2026

Dicyclohexylcarbodiimide → HCID 53851693, compound

https://huagongshe.com/reaction/1982502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantTrimetazidineHCID 21109—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantTetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
ReactantN-Boc-L-Leucine HydrateHCID 12373896—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 53851693HCID 5385169399%

Reaction Steps

Under cooling with ice, a methylene chloride solution (30 ml) of N,N'-dicyclohexylcarbodiimide (41.2 g) was added dropwise to a methylene chloride solution (70 ml) containing tert-butoxycarbonyl-L-leucine monohydrate (4.98 g) and N-hydroxy succinimide (2.30 g), and the mixture was stirred at room temperature for 4 hours. While cooling again with ice, 1-(2,3,4-trimethoxyphenylmethyl)piperazine=dihydrochloride (6.79 g) was added, and triethylamine (8.5 ml) was then added dropwise. The mixture was stirred overnight at room temperature. After removal of methylene chloride by distillation under reduced pressure, ethyl acetate was added to the residue, and any insoluble matters were removed by filtration. The filtrate was washed first with an aqueous sodium bicarbonate solution and then with an aqueous saturated sodium chloride solution, dried over sodium sulfate and distilled under reduced pressure to remove the solvent, whereupon a crude reaction mixture was obtained as an oily viscous substance. This substance was purified by silica gel column chromatography (developing solvent:chloroform:methanol=20:1) to yield 9.5 g of tert-butyl (s)-3-methyl-1-[4-(2,3,4-trimethoxyphenylmethyl)-piperazine-1-yl carbonyl]butylcarbamate as a colorless oily viscous substance (yield: 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04596803
Source datasetuspto-grants-1986_06
ORD IDord-f407851b83b949c2bb8b9b6fbd3b8a56
Source noteuspto-grants-1986_06