N-{4-[4-(1-benzyl-1H-indazol-5-ylamino)-quinazolin-6-yl]-thiazol-2-ylmethyl}-2,2,2-trifluoro-N-(2-methanesulfonyl-ethyl)-acetamide

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Chemical Name:N-{4-[4-(1-benzyl-1H-indazol-5-ylamino)-quinazolin-6-yl]-thiazol-2-ylmethyl}-2,2,2-trifluoro-N-(2-methanesulfonyl-ethyl)-acetamide
CAS No.:659747-69-0
Molecular Formula:C₃₁H₂₆F₃N₇O₃S₂
Molecular Weight:665.72
Hs Code.:

<i>N</i>-{4-[4-(1-benzyl-1<i>H</i>-indazol-5-ylamino)-quinazolin-6-yl]-thiazol-2-ylmethyl}-2,2,2-trifluoro-<i>N</i>-(2-methanesulfonyl-ethyl)-acetamide

Synonyms:N-{4-[4-(1-benzyl-1H-indazol-5-ylamino)-quinazolin-6-yl]-thiazol-2-ylmethyl}-2,2,2-trifluoro-N-(2-methanesulfonyl-ethyl)-acetamide

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Chemical Property of N-{4-[4-(1-benzyl-1H-indazol-5-ylamino)-quinazolin-6-yl]-thiazol-2-ylmethyl}-2,2,2-trifluoro-N-(2-methanesulfonyl-ethyl)-acetamide

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Technology Process of N-{4-[4-(1-benzyl-1H-indazol-5-ylamino)-quinazolin-6-yl]-thiazol-2-ylmethyl}-2,2,2-trifluoro-N-(2-methanesulfonyl-ethyl)-acetamide

There total 7 articles about N-{4-[4-(1-benzyl-1H-indazol-5-ylamino)-quinazolin-6-yl]-thiazol-2-ylmethyl}-2,2,2-trifluoro-N-(2-methanesulfonyl-ethyl)-acetamide 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:

: 98556-31-1
4-chloro-6-iodoquinazoline

: 659747-69-0
N-{4-[4-(1-benzyl-1H-indazol-5-ylamino)-quinazolin-6-yl]-thiazol-2-ylmethyl}-2,2,2-trifluoro-N-(2-methanesulfonyl-ethyl)-acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: propan-2-ol

2: Pd(PPh₃)2Cl₂

3: NBS / CH₂Cl₂

4: dimethylformamide / 70 °C

With bis-triphenylphosphine-palladium(II) chloride; N-Bromosuccinimide; In dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol; 4: Hantzsch reaction;
DOI:10.1016/S0960-894X(02)01047-8

Reference yield:

: 552334-85-7
(2-methylsulfanyl-ethylamino)-acetonitrile

: 659747-69-0
N-{4-[4-(1-benzyl-1H-indazol-5-ylamino)-quinazolin-6-yl]-thiazol-2-ylmethyl}-2,2,2-trifluoro-N-(2-methanesulfonyl-ethyl)-acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / Et₃N / CH₂Cl₂

2: 74 percent / oxone; aq. NaOH

3: 97 percent / H₂S; Et₃N / tetrahydrofuran

4: dimethylformamide / 70 °C

With Oxone; sodium hydroxide; hydrogen sulfide; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; 4: Hantzsch reaction;
DOI:10.1016/S0960-894X(02)01047-8

Reference yield:

: 552334-86-8
N-cyanomethyl-2,2,2-trifluoro-N-(2-methylsulfanyl-ethyl)-acetamide

: 659747-69-0
N-{4-[4-(1-benzyl-1H-indazol-5-ylamino)-quinazolin-6-yl]-thiazol-2-ylmethyl}-2,2,2-trifluoro-N-(2-methanesulfonyl-ethyl)-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: 74 percent / oxone; aq. NaOH

2: 97 percent / H₂S; Et₃N / tetrahydrofuran

3: dimethylformamide / 70 °C

With Oxone; sodium hydroxide; hydrogen sulfide; triethylamine; In tetrahydrofuran; N,N-dimethyl-formamide; 3: Hantzsch reaction;
DOI:10.1016/S0960-894X(02)01047-8