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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979211Generated: October 29, 2026

N,N-Dimethylglycine → HCID 86756903, compound

https://huagongshe.com/reaction/1979211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylglycineHCID 673—
ReactantEthylmorpholineHCID 7525—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(E)-2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)-carbamoyl]-4-phenyl-3-butenyl]-2'-isobutyl-4-methylvalerohydrazideHCID 86756879—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 86756903HCID 86756903—

Reaction Steps

A solution of 0.155 g of N,N-dimethylglycine in 10 ml of dimethylformamide was treated in sequence with 0.167 ml of N-ethylmorpholine, 0.216 g of 1-hydroxybenzotriazole and 0.307 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride. Stirring was continued for 1 hour at room temperature and then 0.459 g of (E)-2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-2′-isobutyl-4-methylvalerohydrazide was added. Stirring was continued overnight and then the mixture was diluted with ethyl acetate and washed in sequence with 5% aqueous sodium hydrogen carbonate and brine. Drying over magnesium sulphate and evaporation gave 0.591 g of (E)-2(R)-[1(S)-(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-2′-isobutyl-4-methyl-2′-[2-(dimethylamino)acetyl]valerohydrazide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239151B1
Source datasetuspto-grants-2001_05
ORD IDord-9de54524f78144e08ae0952a94019949
Source noteuspto-grants-2001_05