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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509774Generated: November 1, 2026

1-Methyl-2-imidazolecarboxaldehyde → HCID 46233761, compound

https://huagongshe.com/reaction/1509774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-2-imidazolecarboxaldehydeHCID 139575—
Reactant4-(2-Aminoethyl)benzenesulfonamideHCID 169682—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantTert-butyl 2-oxoacetateHCID 10986247—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
ProductHCID 46233761HCID 46233761—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4-(2-aminoethyl)benzenesulfonamide (1.40 g, 7.0 mmol), AcOH (0.30 mL) and 1-methyl-1H-imidazole-2-carboxaldehyde (0.77 g, 7.0 mmol) in DCE (40 mL) was heated at 80° C. for 30 min under nitrogen. The reaction mixture was cooled to 0° C., and treated sequentially with NaBH(OAc)3 (4.45 g, 21 mmol) and tert-butyl glyoxalate (1.80 g). The reaction mixture was stirred at room temperature overnight and quenched with water. The reaction mixture was then extracted with DCM and the organic layer was dried and concentrated under reduced pressure. The residue obtained was purified by flash chromatography over silica gel to tert-butyl 2-(((1-methyl-1H-imidazol-2-yl)methyl)(4-sulfamoylphenethyl)amino)acetate (0.63 g, 22%). 1H NMR (400 MHz, DMSO-d6) δ 7.65 (d, J=8.4 Hz, 2 H), 7.26 (s, 2 H), 7.21 (d, J=8.0 Hz, 2 H), 6.99 (d, J=0.8 Hz, 1 H), 6.73 (d, J=0.8 Hz, 1 H), 3.76 (s, 2 H), 3.38 (s, 3 H), 3.28 (s, 2 H), 2.79 (t, J=7.2 Hz, 2 H), 2.69 (t, J=6.8 Hz, 2 H), 1.40 (s, 9 H); ESMS m/z: 409 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211402B2
Source datasetuspto-grants-2012_07
ORD IDord-6dc895a289b44da4beb4c5e2b23bb9e2
Source noteuspto-grants-2012_07