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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480944Generated: October 26, 2026

4-Aminobenzonitrile → HCID 178462395, compound

https://huagongshe.com/reaction/480944

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminobenzonitrileHCID 13396—
ReactantTrimethylaluminumHCID 16682925—
ReactantHCID 178497886HCID 178497886—
ProductHCID 178462395HCID 17846239575%

Reaction Steps

In the same manner as that described in Example 3(4) a reaction was carried out using commercially available 4-aminobenzonitrile (98 mg, 0.83,mmol), trimethylaluminium (0.78 ml, 1.07M n-hexane solution, 0.83 mmol) and methyl 4-[trans-5-[[(1R,2R)-2-(2,4-difluorophenyl)-2-hydroxy-1-methyl-3-(1H-1,2,4-triazol-1-yl)propyl]thio]-1,3-dioxan-2-yl]-3-fluorobenzoate (109 mg, 0.21 mmol) obtained in Example 5(2) and the reaction mixture was treated using a similar procedure to that described in Example 3(4) to give the title compound (95 mg, yield 75%) as a colorless oil which was recrystallized from ethyl acetate-hexane to give white powdery crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06653330B2
Source datasetuspto-grants-2003_11
ORD IDord-d2acf36c55e844f4ad4cacb3b4c6f39b
Source noteuspto-grants-2003_11