HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472320Generated: October 27, 2026
1-(4-Bromophenyl)-4-methylpiperazine → [8-(3-Methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[4-(4-methyl-piperazin-1-yl)-phenyl]-amine
https://huagongshe.com/reaction/472320
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(4-Bromophenyl)-4-methylpiperazine | HCID 11817675 | — |
| Reactant | 2,2'-Bis(dicyclohexylphosphino)-1,1'-biphenyl | HCID 24946987 | — |
| Reactant | 8-(3-(Methylsulfonyl)phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-amine | HCID 57502374 | — |
| Product | [8-(3-Methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[4-(4-methyl-piperazin-1-yl)-phenyl]-amine | HCID 68777407 | — |
Reaction Steps
[8-(3-Methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-[4-(4-methyl-piperazin-1-yl)-phenyl]-amine was prepared from 8-(3-methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine (75.0 mg, 0.260 mmol) and 1-(4-bromo-phenyl)-4-methyl-piperazine (80.0 mg, 0.314 mmol) with 2,2′-bis-dicyclohexylphosphanyl-biphenyl (30.0 mg, 0.0549 mmol) as the ligand in a manner analogous to Step 2d and was isolated as a yellow foam (0.068 g, 56%). 1H NMR (400 MHz, CDCl3, δ, ppm): 8.66 (s, 1H), 8.45 (d, J=6.5 Hz, 1H), 8.38 (d, J=7.7 Hz, 1H), 7.99 (d, J=7.7 Hz, 1H), 7.73 (d, J=6.9 Hz, 1H), 7.66 (d, J=7.4 Hz, 1H), 7.50 (d, J=7.7 Hz, 1H), 7.00-6395 (m, 3H), 6.70 (s, 1H), 3.19-0.314 (m, 4H), 3.12 (s, 3H), 2.62-2.57 (m, 4H), 2.36 (s, 3H). MS=463 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633173B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-4def5f62be7d4ae5a92d84d4b893d002 |
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| Source note | uspto-grants-2014_01 |
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