HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987613Generated: October 30, 2026
4-Aminothiophenol → HCID 178440359, compound
https://huagongshe.com/reaction/1987613
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminothiophenol | HCID 14510 | — |
| Reactant | HCID 178440352 | HCID 178440352 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178440359 | HCID 178440359 | — |
Reaction Steps
(Z)-4-(4-chloroquinolin-2(1H)-ylidene)-3-propyl-1H-pyrazol-5(4H)-one (0.045 g, 0.013 mmol) was dissolved in ethanol (1.5 mL) and 4-aminothiophenol (0.017 g, 0.013 mmol) was added. The reaction mixture was heated to 180° C. using a microwave reactor for 5-10 minutes. The mixture was then concentrated and purified by LC-MS to give Example 25. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.78 (t, J=7.45 Hz, 3H) 1.30-1.40 (m, 2H) 2.22-2.32 (m, 2H) 6.77 (d, J=8.34 Hz, 3H) 7.33 (d, J=8.59 Hz, 2H) 7.60 (t, J=7.33 Hz, 1H) 7.82-7.92 (m, 2H) 8.12 (d, J=8.08 Hz, 1H); ESI-MS: m/z calc'd for C21H20N4OS 376.47. found 377.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07550598B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-db6636447be44e5b8f4f68abd0d0caf6 |
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| Source note | uspto-grants-2009_06 |
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