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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274153Generated: October 27, 2026

2-Chloro-5-methoxy-1H-benzimidazole → HCID 178488095, compound

https://huagongshe.com/reaction/1274153

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-methoxy-1H-benzimidazoleHCID 519197—
Reactant4-(Piperidin-4-ylamino)benzoic Acid tert-Butyl EsterHCID 10636207—
Solvent1-PentanolHCID 6276—
ProductHCID 178488095HCID 17848809583.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

2-Chloro-5-methoxybenzimidazole (0.089 g, 0.49 mmol) was added to a solution of (49) (0.14 g, 0.5 mmol) in n-pentanol (3 mL) at 25° C. The mixture was heated to 120° C. and was maintained at that temperature for 12 h. The reaction mixture was cooled to room temperature and the desired product was filtered and rinsed with acetone to give 0.17 g (83.3%) of the title compound: TLC (Rf =0.30; 5% MeOH/CH2Cl2); 1H NMR (DMSO) δ 13.40 (br s, 1H), 7.63 (d, 2H, J=8.3), 7.29 (d, 1H, J=8.7), 6.91 (s, 1H), 6.83 (d, 1H, J=8.4), 6.65 (d, 2H, J=8.3), 6.50 (s, 1H), 4.13 (d, 2H, J=12.7), 3.77 (s, 3H), 3.73 (m, 1H), 3.47 (m, 4H), 2.06 (d, 2H, J=11.0), 1.48 (s, 9H); 13C NMR (DMSO) δ 165.2, 156.1, 151.3, 149.8, 131.0, 130.9, 124.0, 117.8, 111.8, 111.3, 110.2, 96.4, 79.0, 55.7, 47.3, 45.6, 30.2, 30.0; HRMS (FAB) m/z 423.2388 (M+H)+ (C24H30N4O3 requires 423.2389); Anal. (C24H30N4O3 ·1HCl·1/2H2O) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156758
Source datasetuspto-grants-2000_12
ORD IDord-5781c3ab317b4723874364f6ee1cc21b
Source noteuspto-grants-2000_12