Toluene-4-sulfonic acid 4-oxo-1-phenyl-1,2,3,4-tetrahydro-quinazolin-2-ylmethyl ester

Base Information

Chemical Name:Toluene-4-sulfonic acid 4-oxo-1-phenyl-1,2,3,4-tetrahydro-quinazolin-2-ylmethyl ester
CAS No.:182679-41-0
Molecular Formula:C₂₂H₂₀N₂O₄S
Molecular Weight:408.478
Hs Code.:

Synonyms:Toluene-4-sulfonic acid 4-oxo-1-phenyl-1,2,3,4-tetrahydro-quinazolin-2-ylmethyl ester

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Chemical Property of Toluene-4-sulfonic acid 4-oxo-1-phenyl-1,2,3,4-tetrahydro-quinazolin-2-ylmethyl ester

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Technology Process of Toluene-4-sulfonic acid 4-oxo-1-phenyl-1,2,3,4-tetrahydro-quinazolin-2-ylmethyl ester

There total 3 articles about Toluene-4-sulfonic acid 4-oxo-1-phenyl-1,2,3,4-tetrahydro-quinazolin-2-ylmethyl 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:

: 91-40-7
2-(phenylamino)benzoic acid

: 182679-41-0
Toluene-4-sulfonic acid 4-oxo-1-phenyl-1,2,3,4-tetrahydro-quinazolin-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) thionyl chloride, 2.) aq. ammonia / 1.) toluene, reflux, 1 h, 2.) toluene, 3 h

2: 60 percent / acetic acid / 20 h / Ambient temperature

3: 84 percent / LiBH₄ / tetrahydrofuran / 1 h

4: 86 percent / pyridine / 24 h

With pyridine; ammonium hydroxide; lithium borohydride; thionyl chloride; In tetrahydrofuran; acetic acid;
DOI:10.1002/jhet.5570330427

Reference yield:

: 66491-84-7
2-(ethoxycarbonyl)-1-phenyl-4(1H)-quinazolinone

: 182679-41-0
Toluene-4-sulfonic acid 4-oxo-1-phenyl-1,2,3,4-tetrahydro-quinazolin-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / LiBH₄ / tetrahydrofuran / 1 h

2: 86 percent / pyridine / 24 h

With pyridine; lithium borohydride; In tetrahydrofuran;
DOI:10.1002/jhet.5570330427

Reference yield:

: 1211-19-4
2-phenylaminobenzamide

: 182679-41-0
Toluene-4-sulfonic acid 4-oxo-1-phenyl-1,2,3,4-tetrahydro-quinazolin-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 60 percent / acetic acid / 20 h / Ambient temperature

2: 84 percent / LiBH₄ / tetrahydrofuran / 1 h

3: 86 percent / pyridine / 24 h

With pyridine; lithium borohydride; In tetrahydrofuran; acetic acid;
DOI:10.1002/jhet.5570330427