Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268504Generated: October 30, 2026

Ethyl Acetate → HCID 178455937, compound

https://huagongshe.com/reaction/268504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantIsobutyl chloroformateHCID 62365—
Reactant5-Oxo-L-prolyl-L-tryptophyl-L-prolineHCID 22788749—
ReactantHCID 178455939HCID 178455939—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
ProductHCID 178455937HCID 178455937—

Reaction Steps

The tripeptide, from part C, Pyr-Trp-Pro (23.3 mmoles) is dissolved in DMF (85 ml) and 3.27 ml (23.3 mmoles) TEA, the solution cooled to -20° (inside the flask, or -35° to -40° in the cooling bath) and kept at this temperature for 15-20 minutes. To this cold solution 3.19 ml of isobutyloxycarbonyl chloride is added and then a time of 30 minutes is allowed for the mixed anhydride to be formed at the same temperature. A solution of Arg-Pro-Gln-Ile-Pro-Pro (16.5 g) in DMF (100 ml) is precooled to about 0° and then added into the solution of the mixed anhydride. At this moment, the pH value is adjusted to 8 with TEA (8.5 ml) while the temperature of 0° is maintained. After 20 to 24 hours at room temperature, the volume of the solvents is reduced to 1/3-1/4 and poured into 20-25 volumes of EtOAc containing 3 % of AcOH. The precipitate is washed thoroughly with EtOAc and then dried in vacuo over KOH overnight to yield the title compound. This material is dissolved in water, sterilized by filtration, and the sterile aqueous solution freeze-dried to a free flowing powder. The powder is reconstituted for injection with water for injection or saline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03947575
Source datasetuspto-grants-1976_03
ORD IDord-e02a60ef8f7446beb49fa3bb0f63bda8
Source noteuspto-grants-1976_03