Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 71034-40-7 | HCID 4962722 | — |
| Reactant | HCID 59684264 | HCID 59684264 | — |
| Product | HCID 59684236 | HCID 59684236 | 94% |
Reaction Steps
A neat mixture of 3-(4-fluoro-3-methoxyphenyl)-7-(4-methoxybenzyloxy)isochromen-1-one (100 mg, 0.25 mmol) and 2-amino-N-tert-butyl acetamide (INTERMEDIATE I.2) (32 mg, 2.46 mmol) was heated at 120° C. for 3 h. The reaction mixture was cooled and partitioned between ethyl acetate and sat. NH4Cl (aq.). The organic layer was washed with brine (1×20 mL), dried (MgSO4) and concentrated in vacuo to afford N-tert-butyl-2-(3-(4-fluoro-3-methoxyphenyl)-7-(4-methoxybenzyloxy)-1-oxo-1H-isoquinolin-2-yl)acetamide (120 mg, 0.23 mmol, 94%) which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906504B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-aeab2679d0594bc0bdb351a1ea1e4fe7 |
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| Source note | uspto-grants-2011_03 |
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