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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227502Generated: October 30, 2026

4-Pyridinecarboxaldehyde → HCID 10454518, compound

https://huagongshe.com/reaction/227502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinecarboxaldehydeHCID 13389—
ReactantSodium borohydrideHCID 4311764—
Reactant7-Amino-3-(morpholin-4-ylsulfonyl)-1H-indole-2-carboxamideHCID 10019136—
SolventMethanolHCID 887—
ProductHCID 10454518HCID 10454518—

Reaction Steps

To a solution of 7-amino-3-(morpholin-4-ylsulfonyl)-1H-indole-2-carboxamide from Example 7 (36 mg, 0.11 mmol) in 1 mL of methanol was added 4-formylpyridine (24 mg, 0.22 mmol). After stirring overnight, sodium borohydride was added (13 mg, 0.33 mmol). After 2 hours, the reaction was quenched with 3N HCl, concentrated in vacuo, taken up in DMF, and purified by preparative reversed phase HPLC. The titled product was obtained as a yellow solid. Proton NMR for the product was consistent with the titled compound. ESI+MS: 416.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560546B2
Source datasetuspto-grants-2009_07
ORD IDord-b2ed350bc6ca458c9a4e8bb066558194
Source noteuspto-grants-2009_07