HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-[(1S)-1-cyclopropylpropyl]-3,5-dichloro-2(1H)-pyrazinone → HCID 10112336, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-[(1S)-1-cyclopropylpropyl]-3,5-dichloro-2(1H)-pyrazinone | HCID 18452801 | — |
| Reactant | 7-Chloro-6-fluoro-5-methoxyindoline | HCID 18452820 | — |
| Product | HCID 10112336 | HCID 10112336 | — |
Reaction Steps
Prepared in a similar fashion as described for Example 413 using 3,5-dichloro-1-[(1S)-1-cyclopropylpropyl]-2(1H)-pyrazinone and 7-chloro-6-fluoro-5-methoxyindoline as the starting materials. mp 127–129° C.; 1H NMR (300 MHz, CDCl3): δ 6.96 (s, 1 H), 6.79 (d, J=7.3 Hz, 1 H), 4.33 (t, J=7.9 Hz, 2 H), 4.11–4.00 (m, 1 H), 3.86 (s, 3 H), 3.08 (t, J=7.7 Hz, 2 H), 1.94–1.74 (m, 2 H), 1.07–0.99 (m, 1 H), 0.92 (t, J=7.3 Hz, 3 H), 0.80–0.73 (m, 1 H), 0.55–0.44 (m, 2 H), 0.34–0.25 (m, 1 H); HRMS (ESI) calcd for C19H21N3O2Cl2F (M+H)+: 412.0995; found m/z 412.1001.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07205306B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-b10c27679b3a4d0397b181862c8abf39 |
| Source note | uspto-grants-2007_04 |