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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177578Generated: October 25, 2026

2,2-Difluoro-1,3-benzodioxole-4-carbonyl chloride → 5-[(2,2-Difluoro-1,3-benzodioxol-4-yl)carbonyl]-1-phenyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine

https://huagongshe.com/reaction/2177578

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Difluoro-1,3-benzodioxole-4-carbonyl chlorideHCID 2774062—
Reactant1-phenyl-1H,4H,5H,6H,7H-imidazo[4,5-c]pyridineHCID 13150256—
SolventChloroformHCID 6212—
Product5-[(2,2-Difluoro-1,3-benzodioxol-4-yl)carbonyl]-1-phenyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridineHCID 8627072380%

Reaction Steps

To a solution of the product of Example 50, Step A (28 mg, 0.141 mmol) and TEA (23 μL, 0.169 mmol) in CHCl3 (1 mL) cooled to 0° C. was added 2,2-difluoro-1,3-benzodioxole-4-carbonyl chloride (34 mg, 0.155 mmol). The reaction was warmed to room temperature and stirred overnight. The crude reaction mixture purified on 12 g SiO2 column with 0-4% NH3/MeOH CH2Cl2 to give the desired compound (43 mg, 80%). MS (ESI): mass calcd. for C20H15F2N3O3, 383.1. m/z found, 384.0 [M+H]+. 1H NMR (400 MHz, CDCl3) δ 7.71-7.39 (m, 4H), 7.36-7.09 (m, 5H), 4.88 (s, 1H), 4.58 (t, J=1.6 Hz, 2H), 4.08 (t, J=5.9 Hz, 2H), 3.66 (t, J=5.6 Hz, 1H), 2.86-2.74 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09066946B2
Source datasetuspto-grants-2015_06
ORD IDord-a8aa5e4893f9436096f9a5a2a84d68e1
Source noteuspto-grants-2015_06