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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705559Generated: October 31, 2026

Water → 1-Phenyl-ethanone-O-(4-amino-5-fluoro-pyrimidin-2-yl)oxime

https://huagongshe.com/reaction/705559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantAcetophenonoximeHCID 69185—
Reactant2-Chloro-5-fluoropyrimidin-4-amineHCID 254372—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1-Phenyl-ethanone-O-(4-amino-5-fluoro-pyrimidin-2-yl)oximeHCID 7493186234%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a magnetically stirred mixture of 4-amino-2-chloro-5-fluoropyrimidine (0.10 g, 0.68 mmol) and acetophenone oxime (0.092 g, 0.68 mmol) in dry DMF (3 mL) in a 5 mL Biotage Iniator microwave vessel was added NaH (0.027 g of a 60 wt. % suspension, 0.68 mmol) under a N2 atmosphere. After gas evolution ceased, the resulting mixture was sealed with a Biotage Initiator microwave septa cap and heated to 100° C. in a Biotage Initiator microwave for 60 min. The contents were poured into a vial with water (5 mL) and CH2Cl2 (5 mL), and neutralized with a few drops of 2NHCl. The phases were separated and the organic extract was dried over MgSO4, filtered, and evaporated under a stream of nitrogen. The crude contents were purified on silica (EtOAc/hexanes gradient) and evaporation of the product fractions gave 0.057 g (34%) of 1-Phenyl-ethanone-O-(4-amino-5-fluoro-pyrimidin-2-yl)oxime as an off-white solid: mp 163-165° C.; 1H NMR (300 MHz, CDCl3) δ 8.04 (d, J=2.6 Hz, 1H), 7.75 (m, 2H), 7.42 (m, 3H), 5.25 (bs, 2H), 2.51 (s, 3H); HPLC-MS (ESI) m/z 247 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174970B2
Source datasetuspto-grants-2015_11
ORD IDord-423757b5f9d14afb869273e25ea8ab6d
Source noteuspto-grants-2015_11