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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231870Generated: October 31, 2026

Methanol → HCID 54556555, compound

https://huagongshe.com/reaction/231870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 3246319HCID 3246319—
ReactantHCID 86743235HCID 86743235—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 54556555HCID 54556555—

Reaction Steps

To a solution of 6.4 succinimidyl-N-(S-benzoylmercaptoacetyl)glycinate in 40 ml of ethanol at 70° C. is added in one portion a solution of 1.008 g of the above D-serylglycine in 10 ml of water at 70° C. The reaction mixture is refluxed for 1 hour and then stirred at room temperature overnight. After evaporation of the solvents the residue is agitated with 25 ml of acetone. The precipitate is removed by filtration. Diethylether is added to the filtrate until precipitation is complete. The precipitate is collected by filtration and washed with diethylether. After drying 1.56 g of a yellowish powder is obtained. To 600 mg of this is added 15 ml of chilled methanol. After agitation during 5 min. the white precipitate is filtered off, washed with cold methanol and dried to obtain 400 mg of S-benzoylmercaptoacetylglycyl-D-serylglycine as a white powder, m.p. 149° C. N.M.R. (DMSO-d6): δ 3.61 (2H, d, CH2 --OH), 3.77 (2H, d, α--CH2 --N), 3.84 (2H, d, δ--CH2 --N), 3.88 (2H, s, S--CH2), 4.38 (1H, dt, CH), 8.03 (1H, d, β--NH), 8.17 (1H, t, α--NH), 8.44 (1H, t, γ--NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04849511
Source datasetuspto-grants-1989_07
ORD IDord-d4ae00b0ba8d4625af207fc163f787e4
Source noteuspto-grants-1989_07