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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082226Generated: November 1, 2026

Hydrochloric Acid → HCID 131717768, compound

https://huagongshe.com/reaction/2082226

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantBoc-His(Tos)-OHHCID 6455010—
ReactantHCID 15755292HCID 15755292—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 131717768HCID 13171776883.4%

Reaction Steps

To a solution of Boc-His(Tos)-OH (0.81 g) in methylene chloride (10 ml) were added NMM (0.22 ml) and isobutyl chloroformate (0.26 ml) successively at -15° C., and the mixture was stirred for ten minutes. On the other hand, a solution of HCl.H-D-Trp(CHO)-Phe-OBzl (1.00 g) in DMF (20 ml) was cooled at -30° C. and thereto was added NMM (0.22 ml). This solution was added to the above mentioned mixture and stirred for two hours at -30° C. After evaporation and extraction with ethyl acetate, the organic layer was washed successively with 2% hydrochloric acid, water, 2% sodium hydrogencarbonate, water and saturated sodium chloride solution, and dried over magnesium sulfate. After evaporation, the residue was subjected to column chromatography on silica gel (100 g) and eluted with a mixture of chloroform and methanol (100:1). The fractions containing the object compound were combined and evaporated. The residue was pulverized with n-hexane, filtered, washed with n-hexane and dried to give Boc-His(Tos)-D-Trp(CHO)-Phe-OBzl (1.42 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05187156
Source datasetuspto-grants-1993_02
ORD IDord-ae2f0ada253f49368f792f299db2c0d5
Source noteuspto-grants-1993_02