2-(4-(morpholine-4-sulfonyl)phenylamino)-quinazolin-7-yl trifluoromethanesulfonate

Base Information

Chemical Name:2-(4-(morpholine-4-sulfonyl)phenylamino)-quinazolin-7-yl trifluoromethanesulfonate
CAS No.:953039-95-7
Molecular Formula:C₁₉H₁₇F₃N₄O₆S₂
Molecular Weight:518.494
Hs Code.:

Synonyms:2-(4-(morpholine-4-sulfonyl)phenylamino)-quinazolin-7-yl trifluoromethanesulfonate

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Chemical Property of 2-(4-(morpholine-4-sulfonyl)phenylamino)-quinazolin-7-yl trifluoromethanesulfonate

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Technology Process of 2-(4-(morpholine-4-sulfonyl)phenylamino)-quinazolin-7-yl trifluoromethanesulfonate

There total 7 articles about 2-(4-(morpholine-4-sulfonyl)phenylamino)-quinazolin-7-yl trifluoromethanesulfonate 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: 70.0%

: 953039-93-5
2-(4-morpholin-4-ylsulfonyl-phenylamino)-quinazolin-7-ol

: 17763-67-6
Phenyl triflate

: 953039-95-7
2-(4-(morpholine-4-sulfonyl)phenylamino)-quinazolin-7-yl trifluoromethanesulfonate

Guidance literature:: With 1-methyl-pyrrolidin-2-one; N-ethyl-N,N-diisopropylamine; at 20 ℃;

Reference yield:

: 22996-21-0
4-methoxy-2-nitro-benzaldehyde

: 953039-95-7
2-(4-(morpholine-4-sulfonyl)phenylamino)-quinazolin-7-yl trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 6 steps

1: hydrogenchloride; iron; acetic acid / ethanol; water / 1 h / 60 - 65 °C

2: 1 h / 160 - 180 °C

3: trichlorophosphate / 6 h / Heating / reflux

4: isopropyl alcohol / 80 °C

5: 1-methyl-pyrrolidin-2-one; sodium thiomethoxide / 4 h / 80 °C

6: 1-methyl-pyrrolidin-2-one; N-ethyl-N,N-diisopropylamine / 20 °C

With 1-methyl-pyrrolidin-2-one; hydrogenchloride; iron; acetic acid; N-ethyl-N,N-diisopropylamine; trichlorophosphate; sodium thiomethoxide; In ethanol; water; isopropyl alcohol;

Reference yield:

: 91099-24-0
2-hydroxy-7-methoxyquinazoline

: 953039-95-7
2-(4-(morpholine-4-sulfonyl)phenylamino)-quinazolin-7-yl trifluoromethanesulfonate

Guidance literature:: Multi-step reaction with 4 steps

1: trichlorophosphate / 6 h / Heating / reflux

2: isopropyl alcohol / 80 °C

3: 1-methyl-pyrrolidin-2-one; sodium thiomethoxide / 4 h / 80 °C

4: 1-methyl-pyrrolidin-2-one; N-ethyl-N,N-diisopropylamine / 20 °C

With 1-methyl-pyrrolidin-2-one; N-ethyl-N,N-diisopropylamine; trichlorophosphate; sodium thiomethoxide; In isopropyl alcohol;