HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 533759Generated: October 29, 2026
2-Methoxyaniline → HCID 46843519, compound
https://huagongshe.com/reaction/533759
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxyaniline | HCID 7000 | — |
| 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 46843519 | HCID 46843519 | 7.1% |
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), o-anisidine (48 mg, 0.39 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 45 (9 mg, 7% yield) as a brown oil. LC-MS (M+H=395, obsd.=395).
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-a5afa2c9fdb64ccf9a068ec9c5b233a3 |
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| Source note | uspto-grants-2014_10 |
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