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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530441Generated: November 2, 2026

HCID 68313002, compound → HCID 68312697, compound

https://huagongshe.com/reaction/1530441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68313002HCID 68313002—
CatalystPalladiumHCID 23938—
CatalystPalladium hydroxideHCID 9942167—
ProductHCID 68312697HCID 6831269757.7%

Reaction Steps

To a solution of 4-benzyloxy-2-[2-(2-isopropyl-5-methyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-1,3a-diazabenzo[e]azulen-8-yloxy]-2-methylbutan-1-ol (29 mg, 0.0568 mmol) in IMS (5 mL) was added 10% Pd/C (5 mg). The reaction mixture was stirred at RT under a hydrogen atmosphere for 4 h. The suspension was then filtered through a pad of Celite® and the filtrate was concentrated in vacuo. To a solution of the residue thus obtained in IMS (5 mL) was added Pd(OH)2/C (10 mg) and the reaction mixture was stirred at RT under a hydrogen atmosphere for 18 h. The suspension was then filtered through a pad of Celite® and the filtrate was concentrated in vacuo. The resulting residue was purified by column chromatography (Si-PCC, gradient 2-10% MeOH in DCM) affording 2-[2-(2-Isopropyl-5-methyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-1,3a-diazabenzo[e]azulen-8-yloxy]-2-methylbutane-1,4-diol as a colorless gum (14 mg, 56%). LCMS: RT 2.39 min [M+H]+ 428.3

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090628B2
Source datasetuspto-grants-2015_07
ORD IDord-3198ea4b240e425486c4751ba40be9f3
Source noteuspto-grants-2015_07