HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751021Generated: October 31, 2026
Water → 4-Methylsulfanyl-2'-nitro-biphenyl-2-ylamine
https://huagongshe.com/reaction/751021
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (2-Aminophenyl)boronic acid | HCID 2773216 | — |
| Reactant | Dioxane Methanol | HCID 21966525 | — |
| Reactant | 4-Iodo-3-nitrothioanisole | HCID 59754580 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | 4-Methylsulfanyl-2'-nitro-biphenyl-2-ylamine | HCID 67403177 | — |
Reaction Steps
A methanol/dioxane (20 mL/5 mL of methanol/dioxane) solution/suspension of 4-iodo-3-nitrothioanisole (1 mmol), Pd(OAc)2 (0.01 mmol) was purged with argon for ˜5 min. To this solution Et3N (3 mmol), and 5 mL of water were added and purged with argon for another 5 min. To the above solution, 2-aminophenyl boronic acid (2 mmol, solution in 5 mL of DMF, purged with argon), was added and the reaction mixture was heated at 70° C. (oil bath temperature) for 2 h. The reaction was monitored by HPLC and LC-MS to follow the product formation. The reaction mixture was then cooled down to room temperature and filtered through diatomaceous earth. The filtrate was concentrated and purified using preparative HPLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07405235B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-a02241a396b04110aadf7100cbfaca84 |
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| Source note | uspto-grants-2008_07 |
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