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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297661Generated: November 2, 2026

tert-Butyl mercaptan → HCID 58585855, compound

https://huagongshe.com/reaction/1297661

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl mercaptanHCID 6387—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Chloro-6-iodoquinoline-3-carbonitrileHCID 22466769—
SolventDimethylformamideHCID 6228—
ProductHCID 58585855HCID 5858585548.7%

Reaction Steps

To the solution of 4-chloro-6-iodo-quinoline-3-carbonitrile (example 14c, 1.0 g, 3.18 mmol) in anhydrous DMF (1 mL) and DIEA (1.67 mL, 9.54 mmol) was added 2-methyl-2-propanethiol (0.72 ul, 6.4 mmol). The mixture was stirred at room temperature for 4 h. The reaction was extracted with methylene chloride (2×100 mL). The combined organic layers were successively washed with water (3×50 mL), dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 70-230 mesh, 0%-50% ethyl acetate in hexanes in 30 min) afforded 4-tert-butylsulfanyl-6-iodo-quinoline-3-carbonitrile (0.57 g, 48%) as a white solid. LC-MS m/e 369 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250515B2
Source datasetuspto-grants-2007_07
ORD IDord-a2db4a1b2bbb4caeb6e498573f955e51
Source noteuspto-grants-2007_07