Synthesis of 3,4-dihydro-4-oxoquinazoline derivatives as potential anticonvulsants

DOI: 10.1021/jm00364a012

Source and publish data:

Journal of Medicinal Chemistry p. 1422 - 1425 (1983)

Update date:2022-09-26

Topics:

Authors:

Vaidya Vaidya

Panos Panos

Kite Kite

Iturrian

Blanton Jr.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1021/jm00364a012

Twenty-three substituted 3,4-dihydro-4-oxoquinalines or 3,4-dihydro-4-oxoazaquinazolines have been synthesized utilizing 2-amino-3-cyano-4,5-dimethylfuran and methyl acrylate as precursors for synthesis of the required substituted anthranilates. Six addit

Full text of DOI:10.1021/jm00364a012

Products guided by the article

Product name:2-Methyl-3-(4-trifluoromethyl-phenyl)-3H-pyrido[3,2-d]pyrimidin-4-one

Cas No:86542-82-7

R&D Labs maybe for 86542-82-7

HEZE KINGVOLT CHEMICAL CO., LTD

Contact:86-573-82118911

Address:Juancheng Industry Park
Shanghai Xinda Pharmaceuticals Co., Ltd.

Contact:86-21-33692333-8008

Address:999 Linxian Road, Jinshan Industrial Park, Shanghai, China
Jitat Company Ltd

Contact:852-27701081

Address:Room 2509, New Tech Plaza, 34 Tai Yau St., San Po Kong, HK
Qingdao Kylin Trading Co., Ltd.

Contact:0086-532-68979884/58972912/68972263/65/88171519

Address:Room 2308,A building International Trade Center No.230 Changjiang Middle Road of Qingdao Economic Development Zone,Shandong,China.
Jiangxi Lanqi Fine Chemical S&T Co., Ltd.

Contact:+86-21-64891143

Address:XinJiShan Industrial Area, Zhangshu City, JiangXi Province, China

Relevant to this article

Queuine Analogues. Their Synthesis and Inhibition of Growth of Mouse L5178Y Cells in Vitro

Doi:10.1021/jm00159a031
(1986)
Doi:10.1016/S0040-4039(01)95950-7
(1973)
Syntheses and Reactions of Pyridazine Derivatives, XVIII: Synthesis of Novel Halogen Containing 5-Aroylpyridazine-4-carboxylic Acids and Phenyl 4-Pyridazinyl Ketones

Doi:10.1002/ardp.19833160607
(1983)
Enantioselective Nucleophilic β-Carbon-Atom Amination of Enals: Carbene-Catalyzed Formal [3+2] Reactions

Doi:10.1002/anie.201606571
(2016)
Room-temperature Negishi cross-coupling of unactivated alkyl bromides with alkyl organozinc reagents utilizing a Pd/N-heterocyclic carbene catalyst

Doi:10.1021/jo051304c
(2005)
A C₂-symmetric, living α-diimine Ni(II) catalyst: Regioblock copolymers from propylene

Doi:10.1021/ja0540021
(2005)

Article Doi