methyl-{6-[2-methyl-5-(3-trifluoromethyl-benzoylamino)-phenylcarbamoyl]-benzothiazol-2-yl}-carbamic acid tert-butyl ester

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Chemical Name:methyl-{6-[2-methyl-5-(3-trifluoromethyl-benzoylamino)-phenylcarbamoyl]-benzothiazol-2-yl}-carbamic acid tert-butyl ester
CAS No.:1024583-37-6
Molecular Formula:C₂₉H₂₇F₃N₄O₄S
Molecular Weight:584.619
Hs Code.:

Synonyms:methyl-{6-[2-methyl-5-(3-trifluoromethyl-benzoylamino)-phenylcarbamoyl]-benzothiazol-2-yl}-carbamic acid tert-butyl ester

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Chemical Property of methyl-{6-[2-methyl-5-(3-trifluoromethyl-benzoylamino)-phenylcarbamoyl]-benzothiazol-2-yl}-carbamic acid tert-butyl ester

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Technology Process of methyl-{6-[2-methyl-5-(3-trifluoromethyl-benzoylamino)-phenylcarbamoyl]-benzothiazol-2-yl}-carbamic acid tert-butyl ester

There total 2 articles about methyl-{6-[2-methyl-5-(3-trifluoromethyl-benzoylamino)-phenylcarbamoyl]-benzothiazol-2-yl}-carbamic acid tert-butyl 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: 53.0%

: 67-56-1
methanol

: 1024583-31-0
{6-[2-methyl-5-(3-trifluoromethyl-benzoylamino)-phenylcarbamoyl]-benzothiazol-2-yl}-carbamic acid tert-butyl ester

: 1024583-37-6
methyl-{6-[2-methyl-5-(3-trifluoromethyl-benzoylamino)-phenylcarbamoyl]-benzothiazol-2-yl}-carbamic acid tert-butyl ester

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran;
DOI:10.1016/j.bmcl.2008.02.079

Reference yield:

: 30069-31-9
N-(3-amino-4-methylphenyl)-3-(trifluoromethyl)benzamide

: 1024583-37-6
methyl-{6-[2-methyl-5-(3-trifluoromethyl-benzoylamino)-phenylcarbamoyl]-benzothiazol-2-yl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 20 °C

2: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 20 °C

With di-isopropyl azodicarboxylate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; HATU; In tetrahydrofuran; N,N-dimethyl-formamide;