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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloro-6-methylthiophenol | HCID 4130239 | — |
| Reactant | HCID 60069826 | HCID 60069826 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 67156729 | HCID 67156729 | 86.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943639B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-8009d6b80d4a45cab54336535313f59f |
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| Source note | uspto-grants-2011_05 |
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