Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | 4-Bromobenzene-1,2-diamine | HCID 323593 | — |
| Product | HCID 178419329 | HCID 178419329 | 77% |
Reaction Steps
To a solution of 4-bromo-benzene-1,2-diamine (0.759 g, 4.06 mmol), BOP (1.381 g, 3.12 mmol), and triethylamine (0.44 mL, 3.12 mmol) in acetonitrile (18 mL) were added dropwise over 2 hours a solution of 4-cyclopropyl-phenoxy)-acetic acid (0.600 g, 3.12 mmol) in acetonitrile (5 mL). The reaction mixture was stirred for 12 hours followed by heating at 80° C. for another 8 hours. The reaction mixture was concentrated under reduced pressure to provide a residue, which was purified by chromatography (silica, hexanes: EtOAc=1:1) to afford the title compound as a yellow solid (0.825 g, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612211B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-64daefd72e9c45eca45386eebc9c7f74 |
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| Source note | uspto-grants-2009_11 |
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