HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969688Generated: October 31, 2026
2-amino-N-(4-tert-butylphenyl)benzamide → HCID 59017446, compound
https://huagongshe.com/reaction/969688
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-amino-N-(4-tert-butylphenyl)benzamide | HCID 335177 | — |
| Reactant | 2-Chloro-1,7-naphthyridine | HCID 20696625 | — |
| Reactant | HCID 178418261 | HCID 178418261 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | HCID 59017446 | HCID 59017446 | — |
Reaction Steps
A mixture of 2-amino-N-(4-tert-butyl-phenyl)-benzamide (Step A, 163 mg, 0.61 mmol), 2-chloro-[1,7]naphthyridine (100 mg, 0.61 mmol), Pd2(dba)3 (6.0 mg, 0.006 mmol), 2-dicyclohexyl phosphino-2′-(N-N-dimethyamino)biphenyl (6.0 mg, 0.015 mmol), and LiN(TMS)2 (1 M solution in THF, 2.3 mL) was heated at 80° C. for 12 h in a sealed tube. The mixture was concentrated in vacuo and the crude material was purified with flash chromatography (SiO2, 20% EtOAc/hexane) and crystallization from EtOH to give the desired compound. MS (ES+): 397.0 (M+H)+. Calc'd for C25H24N4O-396.48.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07307088B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-6e5e5080d11a46ce9d0993eba20b20d5 |
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| Source note | uspto-grants-2007_12 |
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