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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366853Generated: October 31, 2026

2,9-Dimethyl-1,10-phenanthroline → 2-Amino-5-[4-(piperidine-1-sulfonyl)-phenylsulfanyl]-isonicotinic acid pentyl ester

https://huagongshe.com/reaction/1366853

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,9-Dimethyl-1,10-phenanthrolineHCID 65237—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 57718193HCID 57718193—
Reactant4-(N-piperidinylsulfonyl)thiophenolHCID 57718290—
CatalystCopper iodideHCID 83717—
SolventTolueneHCID 1140—
Product2-Amino-5-[4-(piperidine-1-sulfonyl)-phenylsulfanyl]-isonicotinic acid pentyl esterHCID 5771821356%

Reaction Steps

Copper iodide (26 mg, 0.14 mmol) and neocuproine (29 mg, 0.14 mmol) were added to a stirred mixture of 2-amino-5-iodo-isonicotinic acid pentyl ester (450 mg, 1.35 mmol), 4-(piperidine-1-sulfonyl)-benzenethiol (449 mg, 1.49 mmol) and sodium t-butoxide (195 mg, 2.025 mmol) in toluene (10 ml) and the reaction was heated to reflux overnight. The reaction was cooled to room temperature, solids filtered off through celite and the filtrate concentrated under reduced pressure onto silica. The residue was purified by flash column chromatography using ethyl acetate 2/3 hexane as eluent to afford 2-amino-5-[4-(piperidine-1-sulfonyl)-phenylsulfanyl]-isonicotinic acid pentyl ester as an orange solid (348 mg, 56%). 1H NMR (CDCl3): (1 H, s, py); 7.51 (2 H, d, Ar); 7.10 (2 H, d, Ar); 6.80 (1 H, s, py); 4.92 (2 H, br s, NH2); 4.14 (2 H, t, OCH2); 2.90 (4 H, m, 2×CH2N pip); 1.53 (6 H, m, OCH2CH2, 2×CH2 pip); 1.46 (2 H, m, CH2 pip); 1.24 (4 H, m, OCH2CH2CH2CHCH3); 0.80 (3 H, t, CH2CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893077B2
Source datasetuspto-grants-2011_02
ORD IDord-e0fd27b96bd04625b6812936125c34ee
Source noteuspto-grants-2011_02