HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044084Generated: November 2, 2026
4-(Methylthio)aniline → HCID 57489635, compound
https://huagongshe.com/reaction/2044084
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Methylthio)aniline | HCID 66038 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 2,6-Dichloropyridine-3-carboxamide | HCID 22142778 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57489635 | HCID 57489635 | 74% |
Reaction Steps
A 1 M THF solution of LiHMDS (6.06 mL, 6.06 mmol) was added dropwise to a mixture of 2,6-dichloronicotinamide (331 mg, 1.733 mmol) and 4-(methylthio)aniline (289 mg, 2.079 mmol) in THF (20 mL) at 0° C. The resulting brown solution was stirred at 0° C. for 5 min, at room temperature for 30 min, quenched with saturated NH4Cl (50 mL) and extracted with EtOAc (3×25 mL). The combined extracts were washed with brine (5 mL), dried (MgSO4), and concentrated. Silica gel chromatography, eluting with 30-70% EtOAc in hexanes, gave the desired product as tan solid (376 mg, 74% yield). LCMS: (M+H)+=293.9. 1H NMR (400 MHz, chloroform-d) δ ppm 10.74 (1H, s), 7.54-7.73 (3H, m), 7.20-7.36 (2H, m), 6.68 (1H, d, J=8.03 Hz), 5.84 (2H, br. s.), 2.48 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586751B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-38bcbe3955564b2d956d0336b2eede16 |
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| Source note | uspto-grants-2013_11 |
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