HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22291565, compound → HCID 22291634, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 22291565 | HCID 22291565 | — |
| Reactant | HCID 22291575 | HCID 22291575 | — |
| Product | HCID 22291634 | HCID 22291634 | — |
Reaction Steps
The title compound was synthesized from 0.30 g of 3-chloro-6-(4-methylpiperazin-1-yl)-2-pyridine carboxylic acid, obtained by acidification of its K-salt from step 1, and the title compound of step 4 of Example 161 (0.217 g) by the same procedure used for Example 260. The title compound is a brown solid (0.23 g, 61%), m.p. 264–266° C. (decomposition). Its structure was confirmed by 1H NMR and LC/MS: 1H NMR (d6-DMSO): δ 2.70 (s, 3H), 2.72–4.30 (m, 12H), 6.02 (s, 2H), 6.92–7.12 (m, 4H), 7.22–7.36 (m, 3H), 7.42–7.53 (m, 2H), 7.77 (d, 1H, J=9 Hz), 10.32 (s, 1H). ESI mass spectrum for C30H29ClN7O4+: 586 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07186743B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-3564be0a0a9c4a4797d02a3f03cb8452 |
| Source note | uspto-grants-2007_03 |