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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979195Generated: November 1, 2026

Acetylglycine → (E)-2'-(2-acetamidoacetyl)-2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-2'-isobutyl-4-methylvalerohydrazide

https://huagongshe.com/reaction/1979195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetylglycineHCID 10972—
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—
Product(E)-2'-(2-acetamidoacetyl)-2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-2'-isobutyl-4-methylvalerohydrazideHCID 8675688378.1%

Reaction Steps

A solution of 0.459 g of (E)-2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-2′-isobutyl-4-methylvalerohydrazide in 4 ml of dimethylformamide was cooled to 0° C. and treated with 0.351 g of N-acetyl-glycine and 690 mg of 1-ethyl-3-(3-dimethylaminopropyl)carbodimide hydrochloride. The mixture was stirred at room temperature for 16 hours and evaporated. The residue in ethyl acetate was washed with 5% sodium hydrogen carbonate solution and water, dried over anhydrous magnesium sulphate and evaporated. The resulting solid was triturated with diethyl ether and filtered off to give 0.436 g of (E)-2′-(2-acetamidoacetyl)-2(R)-[1(S)-[(tetrahydro-2(RS)-pyranyloxy)carbamoyl]-4-phenyl-3-butenyl]-2′-isobutyl-4-methylvalerohydrazide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06239151B1
Source datasetuspto-grants-2001_05
ORD IDord-f56b06ae085643ab9c8eda07b0b43eef
Source noteuspto-grants-2001_05