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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424903Generated: October 30, 2026

Dibenzyl ether → HCID 178484195, compound

https://huagongshe.com/reaction/424903

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 numberUS08106083B2
Source datasetuspto-grants-2012_01
ORD IDord-7bc0e1383ee2413895c2a09e65442f0f
Source noteuspto-grants-2012_01