Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418855Generated: November 2, 2026

Sodium Hydroxide → HCID 178512039, compound

https://huagongshe.com/reaction/1418855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantN-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide esterHCID 76926—
ReactantDL-MalateHCID 160434—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178478772HCID 178478772—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178512039HCID 178512039—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of the product of Example 1, step (b) (1.0 g; 0.0036 moles) in 5.0 ml of water and 5.0 ml of dioxane was added sodium bicarbonate (0.15 g; 0.0018 moles) the reaction then cooled to 0° C. To the stirred solution was added the compound Boc-Gly-OSu, wherein Boc represents benzyloxycarbonyl and OSu represents hydroxysuccinate, (1.1 g; 0.0036 moles) (Novabiochem) and the reaction allowed to warm to room temperature for 18 hrs. The reaction was then poured into 75 ml of water and 20 ml of 2N sodium hydroxide. The aqueous phase was then extracted 3×50 ml of ethyl acetate, and the combined organic extracts were dried over magnesium sulfate. Evaporation of the solvent gave a crude solid which was slurried in 25 ml of ethyl acetate and 75 ml of hexane. The resulting solids were collected by filtration and dried at 20° C. for 24 hrs to give N-(3-(((((phenylmethoxy)carbonyl)amino)methyl)carbonyl)aminophenyl)-1-pyrrolidinecarboximidamide, M.P. 81°-82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885985
Source datasetuspto-grants-1999_03
ORD IDord-85ceeb8b8d074d0a890349a5c043d8a3
Source noteuspto-grants-1999_03