成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

82619-63-4

2-CHLORO-5-FURAN-2-YL-PYRAZINE synthesis

2synthesis methods
-

Yield:82619-63-4 45%

Reaction Conditions:

with trichlorophosphate for 3 h;Heating / reflux;

Steps:

1.C (4-Cyclobutyl-[1,4]diazepan-1-yl)-[5-(4-fluoro-phenoxy)-pyrazin-2-yl]-methanone

Step C: 2-Chloro-5-furan-2-yl-pyrazine. A solution of 5-furan-2-yl-pyrazin-2-ol (7.20 g, 44.4 mmol) in POCl3 (60 mL) was heated at reflux for 3 h. The reaction was allowed to cool, and excess POCl3 was removed by rotary evaporation. The residue was quenched with ice and water. The acidic mixture was basified with aqueous NaOH to pH 10, and the product was extracted with CHCl3. The combined organic extracts were dried (Na2SO4) and concentrated to provide the title chloropyrazine (3.62 g, 45%). 1H NMR (500 MHz, CDCl3): δ 8.73 (d, J=1.4 Hz, 1H), 8.52 (d, J=1.4 Hz, 1H), 7.60 (d, J=1.7 Hz, 1H), 7.14 (d, J=3.4 Hz, 1H), 6.58 (dd, J=3.5, 1.8 Hz, 1H).

References:

US2009/131416,2009,A1 Location in patent:Page/Page column 9