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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552598Generated: October 31, 2026

2-Chlorobenzaldehyde → HCID 23072928, compound

https://huagongshe.com/reaction/552598

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 numberUS07951830B2
Source datasetuspto-grants-2011_05
ORD IDord-62cd524e87364a2a89ef0e0772111688
Source noteuspto-grants-2011_05