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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599296Generated: October 29, 2026

Sodium Hydroxide → HCID 86629453, compound

https://huagongshe.com/reaction/599296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-Fluoro-3-nitroanilineHCID 67768—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86629452HCID 86629452—
SolventAcetic AcidHCID 176—
ProductHCID 86629453HCID 8662945365%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-(tert-butylamino)-6-chloronicotinaldehyde (4.0 g, 18.9 mmol), 4-fluoro-3-nitroaniline (2.9 g, 18.9 mmol) and NaBH(OAc)3 (7.1 g, 37.8 mmol) in CH3COOH (80 mL) was heated to 80° C. for 10 h. The reaction was concentrated under reduced pressure to give a sticky solid, which was suspended in ice water. The mixture was neutralized (pH 7) with 2N aqueous NaOH solution and was extracted with EtOAc. The extracts were washed with brine, dried Na2SO4) and concentrated in vacuo. Purification of the residue by chromatography provided N-tert-butyl-2-chloro-5-((4-fluoro-3-nitrophenylamino)methyl)pyridin-4-amine (4.3 g, 65% yield). 1H NMR (400 MHz, DMSO-d6): δ 7.87 (s, 1 H), 7.32 (m, 1 H), 7.27 (m, 1 H), 7.04 (m, 1 H), 6.68 (s, 1 H), 6.52 (m, 1 H), 5.46 (s, 1 H), 4.17 (d, J=4.8 Hz, 2 H), 1.36 (s, 9 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897762B2
Source datasetuspto-grants-2011_03
ORD IDord-7f3f0e51df134a5ebea7cdfbff0ebf68
Source noteuspto-grants-2011_03