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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524051Generated: October 25, 2026

(6-Chloro-4-(methylamino)pyridin-3-yl)methanol → 6-Chloro-4-(methylamino)nicotinaldehyde

https://huagongshe.com/reaction/524051

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Chloro-4-(methylamino)pyridin-3-yl)methanolHCID 51000240—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product6-Chloro-4-(methylamino)nicotinaldehydeHCID 2343457187.8%

Reaction Steps

A mixture of (6-chloro-4-(methylamino)pyridin-3-yl)methanol (4.2 g, 24.7 mmol) and manganese(IV) oxide (active, 25.8 g, 296.6 mmol) in dichloromethane (50 mL) and THF (50 mL) was stirred at RT overnight. LCMS showed the reaction was completed. The solid was filtered off, and the filtrate was concentrated to afford the title compound (3.7 g, crude) as a light yellow solid, which was directly used in the next step without further purification. MS (ES+) C7H7ClN2O requires: 170, 172. found: 171, 173 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340514B2
Source datasetuspto-grants-2016_05
ORD IDord-91f62f4b2cc8480080b516bf35366868
Source noteuspto-grants-2016_05