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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623675Generated: October 30, 2026

[3-(2,4-bis-benzyloxy-5-isopropyl-phenyl)-3H-[1,2,3]triazol-4-yl]-(4-morpholin-4-yl-phenyl)-carbamic acid t-butyl ester → [3-(2,4-dihydroxy-5-isopropyl-phenyl)-3H-[1,2,3]triazol-4-yl]-(4-morpholin-4-yl-phenyl)-carbamic acid t-butyl ester

https://huagongshe.com/reaction/623675

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[3-(2,4-bis-benzyloxy-5-isopropyl-phenyl)-3H-[1,2,3]triazol-4-yl]-(4-morpholin-4-yl-phenyl)-carbamic acid t-butyl esterHCID 117678191—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Product[3-(2,4-dihydroxy-5-isopropyl-phenyl)-3H-[1,2,3]triazol-4-yl]-(4-morpholin-4-yl-phenyl)-carbamic acid t-butyl esterHCID 131735186—

Reaction Steps

Pd(OH)2/C (0.02 mmol) was added to [3-(2,4-bis-benzyloxy-5-isopropyl-phenyl)-3H-[1,2,3]triazol-4-yl]-(4-morpholin-4-yl-phenyl)-carbamic acid t-butyl ester (135 mg, 0.2 mmol) dissolved in EtOH (5 ml) and the mixture was subjected to one atmosphere of H2 for 1 hour. The catalyst was filtered off through Celite® pad and ethanol was removed under reduced pressure. The crude reaction mixture was used in the next reaction without any purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302998B2
Source datasetuspto-grants-2016_04
ORD IDord-70190a3af3524674b44aaf43e628926f
Source noteuspto-grants-2016_04