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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449814Generated: October 30, 2026

Dibenzyl ether → HCID 178484195, compound

https://huagongshe.com/reaction/449814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenzyl etherHCID 7657—
ReactantHCID 178438831HCID 178438831—
ProductHCID 178484195HCID 178484195—

Reaction Steps

The benzylether [4-(1-(2-aminoethyl)-1H-indol-5-yl)-5-(2,4-bis(benzyloxy)-5-isopropylphenyl)-4H-1,2,4-triazol-3-ol; 188 mg, 0.33 mmol) was dissolved in 6 ml degassed THF/methanol (1:1). 50 mg Pd/C (10%) was added and the mixture stirred under hydrogen (balloon) at rt for 5 h. After filtration the solvent was removed and the crude purified by chromatography on silica with DCM/MeOH (5-20%)/NH4OH (0.5%) to yield 71 mg (0.18 mmol) 4-(5-hydroxy-4-(1-(2-(methylamino)ethyl)-1H-indol-5-yl)-4H-1,2,4-triazol-3-yl)-6-isopropylbenzene-1,3-diol. This amine (50 mg, 0.125) was added to 4-(2,5-dioxopyrrolidin-1-yl)butanoic acid (26 mg, 0.14 mmol), EDC (38 mg, 0.2 mmol) and HOBt (27 mg, 0.2 mmol) in 1.5 ml DMF at rt. The mixture was stirred for 12 h and then ethyl acetate and water added. The aq. Phase was extracted twice with ethyl acetate and the combined organic extracts washed with brine and dried over MgSO4. The crude was purified by chromatography on silica with DCM/MeOH (3-10%) to yield 34 mg (0.061 mmol) product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486932B2
Source datasetuspto-grants-2013_07
ORD IDord-ceb69c6ba5b94bb6a5ba288d2f8efe51
Source noteuspto-grants-2013_07