HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668761Generated: November 2, 2026
1,3-Benzodioxol-5-amine → HCID 57825008, compound
https://huagongshe.com/reaction/1668761
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Benzodioxol-5-amine | HCID 84310 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 57825045 | HCID 57825045 | — |
| Reactant | HCID 67346612 | HCID 67346612 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57825008 | HCID 57825008 | — |
Reaction Steps
An oven dried pressure tube was charged with (RS)-4-(3-bromo-phenyl)-4-phenyl-4,5-dihydro-oxazol-2-ylamine (Building Block A, 100 mg, 0.315 mmol), sodium tert-butoxide (61 mg, 0.63 mmol), 2-di-t-butylphosphino-2′,4′,6′-tri-1-propyl-1,1′biphenyl (12 mg, 0.028 mmol), tris(dibenzylideneacetone)dipalladium (7 mg, 0.008 mmol) and 3,4-(methylendioxy)-aniline (86 mg, 0.631 mmol). After three vacuum-nitrogen cycles, toluene was introduced (0.7 mL), the tube was scaled and stirred at 100° C. for 16 hours. After cooling to room temperature, water (1 mL) and ethyl acetate (1 mL) were added. The organic fraction of the reaction mixture was placed on an SCX column. This was then washed with dichloromethane/methanol. The desired product was obtained by eluting with 2M ammonia in methanol. Fractions containing the compound were combined and the product purified further using preparative HPLC to yield 32 mg (26% yield) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989449B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-928fe12860344940bee8e5e0007dca6d |
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| Source note | uspto-grants-2011_08 |
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