7-methoxy-3-(4-methoxy-phenyl)-4-oxo-3,4-dihydro-quinazoline-5-carboxylic acid methyl ester

Base Information

Chemical Name:7-methoxy-3-(4-methoxy-phenyl)-4-oxo-3,4-dihydro-quinazoline-5-carboxylic acid methyl ester
CAS No.:887468-79-3
Molecular Formula:C₁₈H₁₆N₂O₅
Molecular Weight:340.335
Hs Code.:

Synonyms:7-methoxy-3-(4-methoxy-phenyl)-4-oxo-3,4-dihydro-quinazoline-5-carboxylic acid methyl ester

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Chemical Property of 7-methoxy-3-(4-methoxy-phenyl)-4-oxo-3,4-dihydro-quinazoline-5-carboxylic acid methyl ester

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Technology Process of 7-methoxy-3-(4-methoxy-phenyl)-4-oxo-3,4-dihydro-quinazoline-5-carboxylic acid methyl ester

There total 8 articles about 7-methoxy-3-(4-methoxy-phenyl)-4-oxo-3,4-dihydro-quinazoline-5-carboxylic acid methyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 84.0%

: 887468-56-6
trifluoro-methanesulfonic acid 7-methoxy-3-(4-methoxy-phenyl)-4-oxo-3,4-dihydro-quinazolin-5-yl ester

: 67-56-1
methanol

: 201230-82-2
carbon monoxide

: 887468-79-3
7-methoxy-3-(4-methoxy-phenyl)-4-oxo-3,4-dihydro-quinazoline-5-carboxylic acid methyl ester

Guidance literature:: With palladium diacetate; triethylamine; diphenylphosphinopropane; In dimethyl sulfoxide; for 17h; Heating;
DOI:10.1021/jm0509389

Reference yield:

: 21577-57-1
2-amino-4,6-dimethoxybenzoic acid

: 887468-79-3
7-methoxy-3-(4-methoxy-phenyl)-4-oxo-3,4-dihydro-quinazoline-5-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: 92 percent / tetrahydrofuran / 0 - 20 °C

2.1: 59 percent / DMAP / N,N-dimethyl-acetamide / 24 h / 110 °C

3.1: 55.1 g / 4 h / Heating

4.1: 48 percent / LiCl / dimethylformamide / 2.5 h / 135 °C

5.1: NaH / dimethylformamide / 1 h / 0 - 20 °C

5.2: 85 percent / dimethylformamide / 1 h / 0 - 20 °C

6.1: 84 percent / Pd(OAc)2; diphenylphosphinopropane; Et₃N / dimethylsulfoxide / 17 h / Heating

With dmap; palladium diacetate; sodium hydride; triethylamine; diphenylphosphinopropane; lithium chloride; In tetrahydrofuran; N,N-dimethyl acetamide; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1021/jm0509389

Reference yield:

: 63920-75-2
1,2-dihydro-5,7-dimethoxy-3,1-benzoxazine-2,4-dione

: 887468-79-3
7-methoxy-3-(4-methoxy-phenyl)-4-oxo-3,4-dihydro-quinazoline-5-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 59 percent / DMAP / N,N-dimethyl-acetamide / 24 h / 110 °C

2.1: 55.1 g / 4 h / Heating

3.1: 48 percent / LiCl / dimethylformamide / 2.5 h / 135 °C

4.1: NaH / dimethylformamide / 1 h / 0 - 20 °C

4.2: 85 percent / dimethylformamide / 1 h / 0 - 20 °C

5.1: 84 percent / Pd(OAc)2; diphenylphosphinopropane; Et₃N / dimethylsulfoxide / 17 h / Heating

With dmap; palladium diacetate; sodium hydride; triethylamine; diphenylphosphinopropane; lithium chloride; In N,N-dimethyl acetamide; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1021/jm0509389