HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(1H-Indol-7-yl)-N-methyl-3-phenyl-propionamide → 3-(3-Methoxy-1H-indazol-6-yl)-N-methyl-3-pyridin-2yl-propionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(1H-Indol-7-yl)-N-methyl-3-phenyl-propionamide | HCID 59831745 | — |
| Reactant | HCID 67355209 | HCID 67355209 | — |
| Product | 3-(3-Methoxy-1H-indazol-6-yl)-N-methyl-3-pyridin-2yl-propionamide | HCID 59831718 | — |
Reaction Steps
3-(3-Methoxy-1H-indazol-6-yl)-N-methyl-3-pyridin-2yl-propionamide CCXLVI was prepared from 3-(3-methoxy-1H-indazol-6-yl)-N-methyl-3-pyridin-2yl-acrylamide using the procedure described for preparation of 3-(1H-Indol-7-yl)-N-methyl-3-phenyl-propionamide XIX (Example 4). The crude product (90% yield) was purified via chiral preparative HPLC by multiple injections onto 20×250 mm Chiralpak AD preparative column using a mixture of 60/40 hexane/isopropanol at 7 ml/min affording the enantiomer CCXLVI-A (αD=−0.269°) and the enantiomer CCXLVI-B (αD=+0.209°).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07803830B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-e9b2dc76abb547ebadd1f7ad65947083 |
| Source note | uspto-grants-2010_09 |