3-(benzyloxy)-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(5-methyl-1,3-thiazol-2-yl)benzamide

Base Information

Chemical Name:3-(benzyloxy)-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(5-methyl-1,3-thiazol-2-yl)benzamide
CAS No.:871657-27-1
Molecular Formula:C₂₇H₃₆N₂O₄SSi
Molecular Weight:512.745
Hs Code.:

Synonyms:3-(benzyloxy)-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(5-methyl-1,3-thiazol-2-yl)benzamide

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Chemical Property of 3-(benzyloxy)-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(5-methyl-1,3-thiazol-2-yl)benzamide

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Technology Process of 3-(benzyloxy)-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(5-methyl-1,3-thiazol-2-yl)benzamide

There total 7 articles about 3-(benzyloxy)-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(5-methyl-1,3-thiazol-2-yl)benzamide 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:

: 7305-71-7
5-methyl-2-thiazol-2-amine

: 871656-63-2
3-[((1S)-2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-1-methylethyl)oxy]-5-[(phenylmethyl)oxy]benzoic acid

: 871657-27-1
3-(benzyloxy)-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(5-methyl-1,3-thiazol-2-yl)benzamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In DMF (N,N-dimethyl-formamide); at 20 ℃; for 72h;

Reference yield:

: 100-39-0
benzyl bromide

: 871657-27-1
3-(benzyloxy)-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(5-methyl-1,3-thiazol-2-yl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / DMF (N,N-dimethyl-formamide) / 20 °C

2: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 16 h / 0 - 20 °C

3: lithium hydroxide; water / tetrahydrofuran / 22 h / 20 - 45 °C

4: N-ethyl-N,N-diisopropylamine; HATU / DMF (N,N-dimethyl-formamide) / 72 h / 20 °C

With lithium hydroxide; di-isopropyl azodicarboxylate; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; HATU; In tetrahydrofuran; DMF (N,N-dimethyl-formamide);

Reference yield:

: 871656-59-6
methyl 3-[((1S)-2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-1-methylethyl)oxy]-5-[(phenylmethyl)oxy]benzoate

: 871657-27-1
3-(benzyloxy)-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(5-methyl-1,3-thiazol-2-yl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: lithium hydroxide; water / tetrahydrofuran / 22 h / 20 - 45 °C

2: N-ethyl-N,N-diisopropylamine; HATU / DMF (N,N-dimethyl-formamide) / 72 h / 20 °C

With lithium hydroxide; water; N-ethyl-N,N-diisopropylamine; HATU; In tetrahydrofuran; DMF (N,N-dimethyl-formamide);