HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533757Generated: October 30, 2026
(4-Aminophenoxy)benzene → HCID 46843517, compound
https://huagongshe.com/reaction/533757
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (4-Aminophenoxy)benzene | HCID 8764 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | HCID 58064817 | HCID 58064817 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 2-Methyl-2-butanol | HCID 6405 | — |
| Product | HCID 46843517 | HCID 46843517 | 26.7% |
Reaction Steps
3-Chloro-5,7,8,9-tetrahydro-dipyrido[2,3-b;3′,4′-d]pyrrole-6-carboxylic acid tert-butyl ester (100 mg, 0.32 mmol), 4-phenoxyaniline (120 mg, 0.65 mmol), Pd(OAc)2 (3 mg, 0.01 mmol), X-Phos (12 mg, 0.03 mmol), and KOH (0.03 ml, 0.97 mmol) were suspended in tert-amyl alcohol (2 mL), and stirred overnight at 95° C. The crude mixture was added directly to a Biotage column. The crude product was purified via Biotage eluting with a gradient of 0 to 100% EtOAc in hexanes to provide 43 (39 mg, 26% yield) as a brown solid. LC-MS (M+H=457, obsd.=457).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853391B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-4cc73b02cc9b43379a6585abe732ca10 |
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| Source note | uspto-grants-2014_10 |
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