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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355473Generated: November 2, 2026

1-Acetylpiperazine → tert-Butyl 4-[(4-acetylpiperazin-1-yl)methyl]-6-methoxypyridin-2-ylcarbamate

https://huagongshe.com/reaction/1355473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AcetylpiperazineHCID 83795—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 4-formyl-6-methoxypyridin-2-ylcarbamateHCID 18506791—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-[(4-acetylpiperazin-1-yl)methyl]-6-methoxypyridin-2-ylcarbamateHCID 18506936—

Reaction Steps

To a solution of tert-butyl 4-formyl-6-methoxypyridin-2-ylcarbamate (15-3, 292 mg, 1.16 mmole) and 1-acetylpiperazine (178 mg, 1.39 mmole) in 2% glacial HOAc in CH2Cl2 (5 mL) was added NaBH(OAc)3 (270 mg, 1.27 mmole) at RT. After 1.5 hr the mixture was quenched with saturated NaHCO3 and extracted with CH2Cl2 (3×). The combined organic layers were dried (MgSO4), filtered, and concentrated. Flash column chromatography (gradient, 0-5% EtOH/EtOAc) gave the titled compound as a white foam. 1H-NMR (500 MHz, CDCl3) δ7.41 (s, 1H), 7.00 (bs, 1H), 6.43 (s, 1H), 3.83 (s, 3H), 3.63 (bs, 2H), 3.46 (bs, 4H), 2.41 (m, 4H), 2.08 (s, 3H), 1.52 (s, 9H); MS (ES) (M+H)+365.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586423B2
Source datasetuspto-grants-2003_07
ORD IDord-1f4e0d0510e4450d856229e2e7e2b6d4
Source noteuspto-grants-2003_07