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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133692Generated: October 30, 2026

2-Chlorobenzaldehyde → HCID 23072928, compound

https://huagongshe.com/reaction/133692

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 23072922HCID 23072922—
SolventMethanolHCID 887—
ProductHCID 23072928HCID 2307292855%

Reaction Steps

2-Chlorobenzaldehyde (0.012 ml, 0.11 mM) was added to 2-[(3-isopropoxy-5-aminobenzoyl)amino]-5-thiazolecarboxylic acid (29 mg 0.09 mM) and 4A molecular sieves (90 mg) in methanol under an inert atmosphere at room temperature. After 1 hr sodium cyanoborohydride (7 mg, 0.11 mM) was added and the reaction mixture stirred for 16 hrs. The reaction mixture was filtered, concentrated in vacuo, the residue stirred with water then extracted with ethyl acetate (3×10 ml). The organic extracts were washed with brine (20 ml), dried (MgSO4), filtered and concentrated in vacuo to give the title compound as a pale yellow solid (22 mg, 55%); 1H nmr (d6-DMSO, δ values): 1.22 (6H, d); 4.36 (2H, m); 4.58 (1H, m); 6.24 (1H, s); 6.47 (1H, m); 6.84 (2H, m); 7.26 (3H, m); 7.37 (2H, m); 7.45 (1H, m); 7.76 (1H, br s). MS [M-CO2H]−400, 402.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390908B2
Source datasetuspto-grants-2008_06
ORD IDord-bf7d9c346574474c8fdf74852798787f
Source noteuspto-grants-2008_06