HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 68496294, compound → HCID 67133415, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 68496294 | HCID 68496294 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67133415 | HCID 67133415 | — |
Reaction Steps
3-(5,6-Dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1yl)-4-(5-(4-methoxyphenyl)-1H-indol-3-yl)pyrrole-2,5-dione, prepared as in Example 33, was reduced with Mg in methanol as described in Example 2, Procedure C, to yield (±)-trans-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1yl)-4-(5-(4-methoxyphenyl)-1H-indol-3-yl)pyrrolidine-2,5-dione. 1H NMR (CD3OD) δ: 2.03-2.22(m, 2H), 2.98(t, J=6.0 Hz, 2H), 3.80(s, 3H), 3.97-4.06(m, 1H), 4.06-4.14(m, 1H), 4.38(d, J=6.8 Hz, 1H), 4.67(d, J=6.8 Hz, 1H), 6.86(d, J=8.4 Hz, 2H), 6.91-7.00(m, 2H), 7.08(s, 2H), 7.17-7.27(m, 4H), 7.31(d, J=8.4 Hz, 1H), 7.37(d, J=8.8 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713969B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-3700acb3b44d427282050e9758873d55 |
| Source note | uspto-grants-2010_05 |