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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457310Generated: October 29, 2026

HCID 22291565, compound → HCID 22291634, compound

https://huagongshe.com/reaction/457310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22291565HCID 22291565—
ReactantHCID 22291575HCID 22291575—
ProductHCID 22291634HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186743B2
Source datasetuspto-grants-2007_03
ORD IDord-3564be0a0a9c4a4797d02a3f03cb8452
Source noteuspto-grants-2007_03