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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929539Generated: October 29, 2026

2-Chlorobenzaldehyde → HCID 25027763, compound

https://huagongshe.com/reaction/1929539

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
Reactant2-Chloro-4-fluorobenzaldehydeHCID 145024—
ReactantNicotinamidine hydrochlorideHCID 202042—
ReactantHCID 178479322HCID 178479322—
ProductHCID 25027763HCID 2502776329%

Reaction Steps

The method of Example 3 was used, wherein 3-pyridinecarboxamidine hydrochloride and 2-chloro-4-fluorobenzaldehyde were separately replaced by 2-amidinopyrazinium hydrochloride and 2-chlorobenzaldehyde to obtain a yellow solid of 0.21 g (yield 29%); 1H-NMR (400 MHz, CDCl3) δ 2.15-2.19 (2H, m, CH2); 2.45-2.85 (4H, s, CH2); 6.19 (1H, s, CH); 7.13-7.40 (4H, m, ArH); 8.27 (1H, s, ArH); 8.51 (H, m, ArH); 8.69 (H, m, ArH); 9.57 (1H, s, NH). MS (EI) 338.2 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188091B2
Source datasetuspto-grants-2012_05
ORD IDord-713156a892804fceb0a1bb322194c3b6
Source noteuspto-grants-2012_05