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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734426Generated: November 1, 2026

691-81-6 → HCID 53778955, compound

https://huagongshe.com/reaction/1734426

Reaction equation

Participants

RoleNameHCIDCharge
Reactant691-81-6HCID 11966077—
ReactantHCID 86743235HCID 86743235—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 53778955HCID 5377895531.6%
ProductHCID 86743235HCID 86743235—

Reaction Conditions

Temperature70 °C

Reaction Steps

Succinimidyl-N-(S-benzoylmercaptoacetyl)glycinate is prepared according to the method described by R. F. Schneider et el, Journal of Nuclear Medicine 25 (2), 223-229 (1984). Glycyl-D-alanine in an amount of 250 mg is dissolved in 15 ml of water and the mixture is heated to 70° C. on a water bath. Meanwhile, 1 g of succinimidyl-N-(S-benzoylmercaptoacetyl)glycinate is dissolved in 40 ml of ethanol and the mixture is heated to 70° C. on a water bath. The solution of glycyl-D-alanine in water is added at once to the said ethanolic solution while stirring magnetically. The mixture is then refluxed for 1 hour. After cooling, the solution is evaporated to dryness under reduced pressure. The solid residue is shaken five times with 15 ml of acetone which is each time filtered off. Benzoylmercaptoacetylglycyl-D-alanine is precipitated from the collected filtrates by the addition of diethylether. The precipiate is filtered off and dried in vacuo over phosphorous pentoxide. In this manner 174 mg (yield 31.6%) of benzoylmercaptoacetylglycyl-D-alanine are obtained as a white crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534497
Source datasetuspto-grants-1996_07
ORD IDord-4aedda11a5a947e68d20174b16841a91
Source noteuspto-grants-1996_07