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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549268Generated: October 30, 2026

2-Chloro-6-methylthiophenol → HCID 67156729, compound

https://huagongshe.com/reaction/549268

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6-methylthiophenolHCID 4130239—
ReactantHCID 60069826HCID 60069826—
CatalystHCID 178418397HCID 178418397—
Solvent1-ButanolHCID 263—
ProductHCID 67156729HCID 6715672986.7%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 4-(7-bromo-isoquinoline-1-yl)-piperazine-1-carboxylic acid, tert-butyl ester (0.5 g, 1.3 mmol), 2-chloro-6-methyl-thiophenol (0.206 g, 1.3 mmol), NatBuO (0.44 g, 4.5 mmol), Pd(PPh3)4 (74 mg, 0.065 mmol) in nBuOH (10 mL) was heated at 110° C., 3 h. The reaction mixture was filtered. The filtrate was concentrated and the residue was dissolved in ethyl acetate. The organic phase was washed with water (50 mL×3), separated and dried (MgSO4), filtered. The volatiles were evaporated and the residue was purified by flash column chromatography (SiO2, n-heptane: ethyl acetate 8:2) to give 530 mg of the title compound as colourless oil (yield 86.4%). 1H NMR (CDCl3) δ 8.05 (d, 1H), 7.65 (d, 1H), 7.20-7.45 (m, 5H), 7.15 (d, 1H), 3.26-3.40 (m, 4H), 3.10-3.20 (m, 4H), 2.5 (s, 3H), 1.38 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943639B2
Source datasetuspto-grants-2011_05
ORD IDord-8009d6b80d4a45cab54336535313f59f
Source noteuspto-grants-2011_05