Hydrochloric Acid → 2-Chloro-4,6-dimethoxypyrimidine

온도

0 °C

1,260 ml of 36% hydrochloric acid were charged in a 5-l four-necked flask and then cooled to 0° C. After 180 g (1.16 moles) of 2-amino-4,6-dimethoxypyrimidine were added in small portions into the flask, the resulting mixture was stirred for about 1 hour until the reaction mixture changed into a syrupy form. After the reaction mixture was cooled to -15° C., 260 ml of 159 g (2.3 moles) of NaNO2 in H2O were added dropwise over about 1 hour under vigorous stirring. After completion of the dropwise addition, the resulting mixture was stirred at -15° to -10° C. for additional 1 hour so that the reaction was brought to completion. While the reaction mixture was retained at -5° C., 1.5 l of a 30% aqueous solution of NaOH were charged dropwise so that the reaction mixture was neutralized to pH 7. By filtration under reduced pressure, a clay-like material of a purple color was collected. The target compound was extracted from the clay-like material using 3 l of ethyl acetate. Through the procedure of washing with water, drying over anhydrous sodium sulfate and removal of the solvent, 63 g of bluish crude crystals were obtained. They were crystallized further by silica get chromatography to obtain 60.8 g of white crystals (yield: 29.9%).

1. temperatureAfter the reaction mixture was cooled to -15° C.
2. additionAfter completion of the dropwise addition
3. stirringthe resulting mixture was stirred at -15° to -10° C. for additional 1 hour so that the reaction
4. customwas retained at -5° C.
5. filtrationBy filtration under reduced pressure
6. customa clay-like material of a purple color was collected
7. extractionThe target compound was extracted from the clay-like material
8. washThrough the procedure of washing with water
9. dry with materialdrying over anhydrous sodium sulfate and removal of the solvent

ORD 기록

ord-a6cf9824225a4bec819a9d194fa5be81

출처 데이터셋

uspto-grants-1991_10

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US05053070