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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202154Generated: October 30, 2026

2-Hydrazinylpyrimidine → HCID 71260694, compound

https://huagongshe.com/reaction/2202154

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-HydrazinylpyrimidineHCID 346558—
ReactantSodium AcetateHCID 517045—
ReactantHCID 86676679HCID 86676679—
SolventAcetic AcidHCID 176—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 71260694HCID 71260694—

Reaction Conditions

Temperature80 °C

Reaction Steps

tert-Butyl 4-{[(4-fluorophenyl)carbonothioyl]-carbamoyl}piperidine-1-carboxylate (0.37 g, 1.01 mmol) was mixed with 2-hydrazinylprimidine (0.13 g, 1.21 mmol) and sodium acetate (0.099 g, 1.21 mmol) in 3 ml of 1,4-dioxane and acetic acid (1:1). After heating at 80° C. for 45 min, the solvents were removed under vacuum. The resulting residue was re-dissolved in dichloromethane and washed with saturated sodium bicarbonate solution and water. The organic layers were concentrated, and the residue was purified by column chromatography using a gradient of 0˜50% ethyl acetate in hexanes. LC-MS (m/z): 369.10 [M−56+H]+, 447.14 [M+Na+H]+. 1HNMR (CDCl3, 500 MHz): δ 8.92 (d, J=4.8 Hz, 2H), 8.25-8.28 (m, 2H), 7.38 (t, J=4.8 Hz, 1H), 7.15 (t, J=8.7 Hz, 2H), 4.24-4.27 (br, 2H), 3.94-4.00 (m, 2H), 2.91-2.96 (br, 2H), 2.00-2.10 (br, 4H), 1.52 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365539B2
Source datasetuspto-grants-2016_06
ORD IDord-3a6e3851060944c7b8c3429b63289b8b
Source noteuspto-grants-2016_06