Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101490Generated: October 31, 2026

Acetone → [1-(3,5-Dichloro-benzyl)-1H-imidazol-2-ylmethyl]-(3-fluoro-benzyl)-isopropyl-amine

https://huagongshe.com/reaction/2101490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 11951591HCID 11951591—
SolventMethanolHCID 887—
Product[1-(3,5-Dichloro-benzyl)-1H-imidazol-2-ylmethyl]-(3-fluoro-benzyl)-isopropyl-amineHCID 1195231026%

Reaction Steps

A mixture of [1-(3,5-dichloro-benzyl)-1H-imidazol-2-ylmethyl]-(3-fluoro-benzyl)-amine, (200 mg, 0.55 mmol), acetone (81 uL, 1.10 mmol) and 3A molecular sieves (300 mg) in MeOH (3 mL) was stirred at ambient temperature under N2. After 5 h, NaBH3CN was added and the mixture stirred for an additional 2 h. Water (2 mL) was added and the reaction mixture concentrated in vacuo. The residue was taken up in 1N NaOH (20 mL) and extracted with CH2Cl2 (3×30 mL). The combined extracts were dried over Na2SO4 and concentrated in vacuo. The crude material was purified by chromatography (silica gel, 100% EtOAc) and the isolated product converted to the di-hydrochloride salt by treatment with excess anhydrous HCl in methanol solution. The volatiles were removed in vacuo to afford the desired product 6a (58 mg, 26%) as an off-white solid: ESI MS m/z 406 [C21H22Cl2FN3+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572921B2
Source datasetuspto-grants-2009_08
ORD IDord-bca050e6ad224eed817f9827ec960fec
Source noteuspto-grants-2009_08