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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914722Generated: October 30, 2026

Acetic Acid → HCID 59352972, compound

https://huagongshe.com/reaction/1914722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthanolHCID 702—
ReactantHCID 57625373HCID 57625373—
ReactantHCID 59353087HCID 59353087—
SolventWaterHCID 962—
ProductHCID 59352972HCID 5935297235%

Reaction Conditions

Temperature90 °C

Reaction Steps

N-(3-chloroquinoxalin-2-yl)-1-methyl-1H-imidazole-4-sulfonamide (1 g; 3.1 mmol; 1 eq) and 4-(2-amino-4-methoxy-benzyl)-piperidine-1-carboxylic acid tert-butyl ester (1.1 g; 3.4 mmol; 1.1 eq) are suspended in water (12.5 mL) and EtOH (12.5 mL) then AcOH (2.5 mL) is added. The resulting suspension is heated up to 90° C. for 3 days. Boc deprotection occurs during the reaction. The solvents are evaporated under reduced pressure and the resulting oily brown residue is taken up in water. An excess triethylamine is added until pH=8 to trap the HCl formed during the reaction. The precipitate is filtered off then washed thoroughly with water until neutral. It is dried under vacuum at 40° C. for 2 days, affording 544 mg (35%) of the title compound as a grey solid. 1H NMR (DMSO-d6) δ 9.35 (s, 1H), 8.70 (d, J=2.4 Hz, 1H), 7.69 (s, 1H), 7.50-7.30 (m, 3H), 7.35-6.97 (m, 3H), 6.48 (dd, J=8.3, 2.7 Hz, 1H), 3.89 (s, 2H), 3.78 (s, 3H), 3.63 (s, 3H), 3.45-3.15 (m, 2H), 2.97-2.78 (m, 2H), 2.65-2.53 (m, 2H), 2.05-1.80 (m, 2H), 1.56-1.32 (m, 2H). HPLC (max plot) 89%; Rt 3.08 min. LC/MS: (ES+) 508.1, (ES−) 506.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614215B2
Source datasetuspto-grants-2013_12
ORD IDord-8fb15243128f43d0b5fbbea587f1c68f
Source noteuspto-grants-2013_12