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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896369Generated: October 29, 2026

Acetyl chloride → 4-[5-Aminomethyl-2-(3-vinyl-indazol-1-ylmethyl)-benzoimidazol-1-yl]-butan-1-ol

https://huagongshe.com/reaction/896369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTrifluoroacetic acidHCID 6422—
Reactant[1-(4-hydroxy-butyl)-2-(3-vinyl-indazol-1-ylmethyl)-1H-benzoimidazol-5-ylmethyl]-carbamic acid tert-butyl esterHCID 69719540—
SolventDichloromethaneHCID 6344—
Product4-[5-Aminomethyl-2-(3-vinyl-indazol-1-ylmethyl)-benzoimidazol-1-yl]-butan-1-olHCID 22349294—

Reaction Steps

To a suspension of [1-(4-hydroxy-butyl)-2-(3-vinyl-indazol-1-ylmethyl)-1H-benzoimidazol-5-ylmethyl]-carbamic acid tert-butyl ester (17 mg, 0.036 mmol) in DCM (1 mL) was added TFA (82 μL, 1.1 mmol). The solution was allowed to stir for 2.5 hrs. followed by the removal of the volatiles in vacuo. The resulting trifluoroacetate was dissolved in methanol (3 mL) followed by the addition of acetyl cloride (26 μL, 0.36 mmol) and concentrated after 10 min. This procedure was repeated once allowing the reaction to run for 3 hrs. The solution was concentrated in vacuo and the residue stripped with DCM (thrice). The product was triturated in diethyl ether and the ether decanted to yield 4-[5-aminomethyl-2-(3-vinyl-indazol-1-ylmethyl)-benzoimidazol-1-yl]-butan-1-ol; HCl salt (10 mg, 67%) as an off white solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919331B2
Source datasetuspto-grants-2005_07
ORD IDord-35bcd555491e4ffe8ee892674acbc5ba
Source noteuspto-grants-2005_07