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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879351Generated: November 2, 2026

2-(3-(methylamino)propyl)-1H-benzimidazole → rac-(1R*,8R*,9R*)-9-(2-{[3-(1H-Benzoimidazol-2-yl)-propyl]-methyl-amino}-ethyl)-tricyclo[6.2.2.02,7]dodeca-2,4,6-trien-9-ol

https://huagongshe.com/reaction/1879351

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-(methylamino)propyl)-1H-benzimidazoleHCID 3145400—
Reactantrac-Toluene-4-sulfonic acid (1R*,8R*,9R*)-2-(9-hydroxy-tricyclo[6.2.2.02,7]dodeca-2,4,6-trien-9-yl)-ethyl esterHCID 87403382—
SolventDiisopropylethylamineHCID 81531—
Productrac-(1R*,8R*,9R*)-9-(2-{[3-(1H-Benzoimidazol-2-yl)-propyl]-methyl-amino}-ethyl)-tricyclo[6.2.2.02,7]dodeca-2,4,6-trien-9-olHCID 70999519—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 1000 mg of rac-toluene-4-sulfonic acid (1R*,8R*,9R*)-2-(9-hydroxy-tricyclo[6.2.2.02,7]dodeca-2,4,6-trien-9-yl)ethyl ester and 508 mg of [3-(1H-benzoimidazol-2-yl)-propyl]-methyl-amine in 2 mL of DIPEA was heated to 110° C. for 30 min. The reaction mixture was cooled to rt, quenched with MeOH-water and extracted with EtOAc. The organic phase was separated, dried over Na2SO4 and concentrated in vacuo to obtain 1.0 g as beige solid. A part of the crude product was purified by CC with EtOAc/MeOH (2:1) to obtain the desired compound as beige foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314253B2
Source datasetuspto-grants-2012_11
ORD IDord-2a1b1248cc314fc5adfe330f093e79c9
Source noteuspto-grants-2012_11