Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301892Generated: October 30, 2026

Sodium Hydroxide → HCID 178448339, compound

https://huagongshe.com/reaction/2301892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178501509HCID 178501509—
SolventMethanolHCID 887—
ProductHCID 178448339HCID 178448339—

Reaction Conditions

Temperature20 °C

Reaction Steps

Two grams (g) of BOC-Gly-D-Arg-Gly-Asp-Phe-Val-OMe (SEQ ID NO 1) were first dissolved in 60 milliliters (ml) of methanol to which was added 1.5 ml of 2 N sodium hydroxide solution to form an admixture. The admixture was then stirred for 3 hours at 20 degrees C. (20 C.). After evaporation, the residue was taken up in water, acidified to pH 3 with diluted HCl and extracted with ethyl acetate. The extract was dried over Na2SO4, evaporated again and the resultant BOC-Gly-D-Arg-Gly-Asp-Phe-Val-OH (SEQ ID NO 2) was stirred at 20 C. for 2 hours with 20 ml of 2 N HCl in dioxane. The resultant admixture was evaporated to obtain H-Gly-D-Arg-Gly-Asp-Phe-Val-OH (SEQ ID NO 3) that was subsequently dissolved in a mixture of 1800 ml of dichloromethane and 200 ml of dimethylformamide (DMF) followed by cooling to 0 C. Thereafter, 0.5 g of dicyclohexylcarbodiimide (DCCI), 0.3 g of 1-hydroxybenzotriazole (HOBt) and 0.23 ml of N-methylmorpholine were added successively with stirring.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500924B1
Source datasetuspto-grants-2002_12
ORD IDord-6843a99bab7c4a7d8cc46fdaf56f3c7a
Source noteuspto-grants-2002_12