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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164877Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 53851693, compound

https://huagongshe.com/reaction/2164877

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 numberUS04507297
Source datasetuspto-grants-1985_03
ORD IDord-59be7f5fc6bf4e25b0d4fd102b4cdb2b
Source noteuspto-grants-1985_03