HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588149Generated: October 29, 2026
2-Methoxyaniline → 6-chloro-3-methoxy-N-(2-methoxyphenyl)-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-amine
https://huagongshe.com/reaction/588149
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methoxyaniline | HCID 7000 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 4,6-dichloro-3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridine | HCID 118272510 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-chloro-3-methoxy-N-(2-methoxyphenyl)-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-amine | HCID 118272439 | — |
Reaction Steps
4,6-dichloro-3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridine (Intermediate 37B, 100 mg, 0.217 mmol), 2-methoxyaniline (26.0 μl, 0.217 mmol), t-butyl X-Phos palladacycle (5.97 mg, 8.69 μmol) were combined in a 5 ml microwave vial. The vial was evacuated and backfilled (3×) with N2 gas before adding THF (2.2 ml) and potassium t-butoxide (326 μl, 0.326 mmol). The reaction was allowed to stir at 80° C. for 2 hours. Room temperature was attained and the mixture was filtered through a celite frit and concentrated in vacuo while loading onto silica gel. Purifcation by MPLC 0-20% EtOAc/DCM gave 6-chloro-3-methoxy-N-(2-methoxyphenyl)-1-trityl-1H-pyrazolo[4,3-c]pyridin-4-amine (52B). MS: [M+H]+ m/z 547.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09226922B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-6329add573864d84849cbb603804ec8a |
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| Source note | uspto-grants-2016_01 |
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