4-Methoxybenzonitrile → 6(4-Methoxyphenyl)-5h-thieno[3,2-c]pyridin-4-one

To a solution of N-methyl-2-methylthiophene-3-carboxamide (36.0 g) in THF (500 ml) was added dropwise 2.5M n-BuLi/THF solution (200 ml) at −70° C. The reaction solution was stirred at −70° C. for 2 hr, followed by the addition of anisonitrile (31.0 g) at once. After the dry ice/acetone bath was removed, the reaction mixture was back to room temperature. Three hours later, an aqueous solution of saturated ammonium chloride and ether were added thereto, and then the mixture was further stirred for 1 hr. The resulting white precipitates were collected by filtration, washed with water, ether and n-hexane in this order, and then dried, to give the title compound (17.9 g, yield; 30%).

1. customAfter the dry ice/acetone bath was removed
2. customwas back to room temperature
3. additionThree hours later, an aqueous solution of saturated ammonium chloride and ether were added
4. stirringthe mixture was further stirred for 1 hr
5. customThe resulting white precipitates
6. filtrationwere collected by filtration
7. washwashed with water, ether and n-hexane in this order
8. customdried

ORDレコード

ord-68edf2d14c8e46e693393f712a601978

出典データセット

uspto-grants-2004_09

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06790844B2