HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424903Generated: October 30, 2026
Dibenzyl ether → HCID 178484195, compound
https://huagongshe.com/reaction/424903
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibenzyl ether | HCID 7657 | — |
| Reactant | HCID 178438831 | HCID 178438831 | — |
| Product | HCID 178484195 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08106083B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-7bc0e1383ee2413895c2a09e65442f0f |
|---|
| Source note | uspto-grants-2012_01 |
|---|