Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255619Generated: November 1, 2026

HCID 20183020, compound → HCID 178445974, compound

https://huagongshe.com/reaction/255619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20183020HCID 20183020—
ReactantHCID 178445973HCID 178445973—
SolventDimethylformamideHCID 6228—
ProductHCID 178445974HCID 17844597475.7%

Reaction Steps

66 mg (0.1 mmole) of 4(S)-[N-benzyloxycarbonyl-3-(1-naphthyl)-L-alanyl-L-histidyl]amino-3(S)-hydroxy-6-methylheptanoic acid hydrazide (prepared as described in Example 5) were dissolved in 3 ml of dimethylformamide, and then 31 mg (0.1 mmole) of N-hydroxysuccinimide 4-benzoylbutyrate were added and the mixture was stirred for 2 days at room temperature. The resulting reaction mixture was concentrated by evaporation under reduced pressure, and water was added to the resulting residue. After the water had been added to the residue, the precipitate was separated by filtration. It was washed with water, and the powder obtained after drying was washed with ethyl acetate, to give 63 mg of the title compound as a white powdery solid melting at 158°-160°, [α]27 -44.4° (C=0.5, methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04698329
Source datasetuspto-grants-1987_10
ORD IDord-1989704b51b74dc6b8040bb340dea39b
Source noteuspto-grants-1987_10