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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197070Generated: November 1, 2026

Hydrochloric Acid → HCID 178462207, compound

https://huagongshe.com/reaction/1197070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsobutyl chloroformateHCID 62365—
ReactantTert-butoxycarbonylalanineHCID 85082—
ReactantHCID 178512188HCID 178512188—
SolventDimethylformamideHCID 6228—
ProductHCID 178462207HCID 17846220770.3%

Reaction Steps

After 15.9 g (0.084 mole) of BOC-Ala-OH was dissolved in 84 ml of DMF, 10.9 ml (0.084 mole) of NEM was added to the solution. Then, 10.9 ml (0.084 mole) of isobutyl chloroformate was dropwise added to the solution at -20° C. The resulting mixture was reacted for 10 minutes. After completion of the reaction, 84 ml of a solution of 32.8 g (0.084 mole) of HCl.H-Arg(NO2)-CHA and 32.8 ml (0.252 mole) of NEM in DMF was dropwise added to the reaction solution at -15° to -10° C. After the dropwise addition, the mixture was reacted at the same temperature for 23 hours and further at room temperature (15° to 20° C.) for 18 hours. After the reaction, DMF was removed by distillation under reduced pressure and the residue was dissolved in 600 ml of AcOEt. After washing 3 times with 200 ml of cold 5% hydrochloric acid and twice with 200 ml of saturated sodium chloride aqueous solution, the solution was dried over anhydrous magnesium sulfate and decolored with activated charcoal. After drying, magnesium sulfate and activated charcoal were filtered off and the solvent was removed by distillation under reduced pressure. Recrystallization of the residue gave 31.0 g (70.3%) of BOC-Ala-Arg(NO2)-CHA.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116941
Source datasetuspto-grants-1992_05
ORD IDord-677fdab12c8a45b1ae2e85e0fbb45e7f
Source noteuspto-grants-1992_05