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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395153Generated: November 3, 2026

HCID 86753148, compound → HCID 14801625, compound

https://huagongshe.com/reaction/2395153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86753148HCID 86753148—
ReactantHCID 86753149HCID 86753149—
CatalystPalladiumHCID 23938—
Solvent1,1,1,3,3,3-Hexafluoro-2-propanolHCID 13529—
ProductHCID 14801625HCID 14801625—

Reaction Steps

100 mg of benzyl 5-[(N-benzyloxycarbonyl-L-valyl-L-alanyl-L-alanyl-L-phenylalanyl-L-leucyl-L-alanyl-L-leucyl-L-alanyl)aminomethyl]-3,6-dimethoxy-9,9-dimethylxanthene-4-acetate (benzyl 5-[(N-benzyloxycarbonyl-SEQ ID NO:9)aminomethyl]-3,6-dimethoxy-9,9-dimethylxanthene-4-acetate) were dissolved in 200 ml of hexafluoroisopropanol, treated with 60 mg of palladium on calcium carbonate (10%) and stirred under hydrogen for 3 hours. After filtering the catalyst the filtrate was concentrated. The residue remaining was washed several times with methanol and thereafter chromatographed over silica gel in chloroform/methanol/hexafluoroisopropanol, whereby 65 mg of 3,6-dimethoxy-9,9-dimethyl-5-[(L-valyl-L-alanyl-L-alanyl-L-phenylalanyl-L-leucyl-L-alanyl-L-leucyl-L-alanyl)aminomethyl]xanthene-4-acetic acid (3,6-dimethoxy-9,9-dimethyl-5-[(SEQ ID NO:9)aminomethyl]xanthene-4-acetic acid) were obtained; IR 3393, 3288, 2963, 1685, 1636, 1531 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811548
Source datasetuspto-grants-1998_09
ORD IDord-fafade14265347488b6060d035d8a834
Source noteuspto-grants-1998_09