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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7794Generated: October 29, 2026

Formaldehyde → 6-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]-N,N-dimethylpyridin-3-amine

https://huagongshe.com/reaction/7794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant6-[4-(1,3-Benzoxazol-2-yl)-2-methoxyphenyl]pyridin-3-amineHCID 10149716—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
Product6-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]-N,N-dimethylpyridin-3-amineHCID 10236912—

Reaction Steps

6-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]pyridin-3-amine (22 mg, 0.070 mmol) was dissolved in MeOH (2 mL), and AcOH (2 drops). NaCNBH3 (44 mg, 0.70 mmol) and formaldehyde (50 μL, 0.70 mmol) were added and the mixture was stirred overnight. The mixture was partitioned between CH2Cl2 and dilute brine. The aqueous layer was extracted with CH2Cl2 (3×15 mL). The combined organic layers were dried over MgSO4, filtered and concentrated. The crude mixture was adsorbed onto silica gel and purified by automated flash chromatography using an EtOAc/hexanes gradient to afford the desired 6-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]-N,N-dimethylpyridin-3-amine: 1H NMR (CDCl3, 300 MHz) δ 8.24–8.23 (d, 1H), 7.94 (s, 2H), 7.87 (s, 1H), 7.84–7.79 (m, 2H), 7.59 (m, 1H), 7.38–7.35 (m, 2H), 7.07–7.06 (m, 1H), 4.01 (s, 3H), 3.04 (s, 6H). MS (ESI) 346 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087601B2
Source datasetuspto-grants-2006_08
ORD IDord-5a63f83402bd4a00a7cdbe18b772ccfe
Source noteuspto-grants-2006_08