N-(N',N'-Dimethylaminoethyl)-4-[N-methyl-N-(tert-butyloxycarbonyl)amino]phenylacetamide

Base Information

Chemical Name:N-(N',N'-Dimethylaminoethyl)-4-[N-methyl-N-(tert-butyloxycarbonyl)amino]phenylacetamide
CAS No.:251643-19-3
Molecular Formula:C₁₈H₂₉N₃O₃
Molecular Weight:335.447
Hs Code.:

Synonyms:N-(N',N'-Dimethylaminoethyl)-4-[N-methyl-N-(tert-butyloxycarbonyl)amino]phenylacetamide

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Chemical Property of N-(N',N'-Dimethylaminoethyl)-4-[N-methyl-N-(tert-butyloxycarbonyl)amino]phenylacetamide

Chemical Property:

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Technology Process of N-(N',N'-Dimethylaminoethyl)-4-[N-methyl-N-(tert-butyloxycarbonyl)amino]phenylacetamide

There total 7 articles about N-(N',N'-Dimethylaminoethyl)-4-[N-methyl-N-(tert-butyloxycarbonyl)amino]phenylacetamide 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:

: 76143-33-4
5-(methoxycarbonyl)-2-nitrobenzoic acid

: 251643-19-3
N-(N',N'-Dimethylaminoethyl)-4-[N-methyl-N-(tert-butyloxycarbonyl)amino]phenylacetamide

Guidance literature:: Multi-step reaction with 7 steps

1: SOCl₂ / dimethylformamide / 3 h / Heating

2: tetrahydrofuran / 0.5 h / -10 °C

3: BH₃*DMS / tetrahydrofuran / 1 h / 20 °C

4: 62 percent / DMAP / tetrahydrofuran / 16 h / Heating

5: 97 percent / LiOH; H₂O / methanol / 0.5 h / 50 °C

6: dimethylformamide / 0.17 h / 50 °C

7: dimethylformamide / 2 h / 20 °C

With dmap; lithium hydroxide; thionyl chloride; dimethylsulfide borane complex; water; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; 1: Substitution / 2: Formylation / 3: Reduction / 4: Substitution / 5: Hydrolysis / 6: Substitution / 7: Acylation;
DOI:10.1039/a904067f

Reference yield:

: 3-Chlorocarbonyl-4-nitro-benzoic acid methyl ester

: 251643-19-3
N-(N',N'-Dimethylaminoethyl)-4-[N-methyl-N-(tert-butyloxycarbonyl)amino]phenylacetamide

Guidance literature:: Multi-step reaction with 6 steps

1: tetrahydrofuran / 0.5 h / -10 °C

2: BH₃*DMS / tetrahydrofuran / 1 h / 20 °C

3: 62 percent / DMAP / tetrahydrofuran / 16 h / Heating

4: 97 percent / LiOH; H₂O / methanol / 0.5 h / 50 °C

5: dimethylformamide / 0.17 h / 50 °C

6: dimethylformamide / 2 h / 20 °C

With dmap; lithium hydroxide; dimethylsulfide borane complex; water; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; 1: Formylation / 2: Reduction / 3: Substitution / 4: Hydrolysis / 5: Substitution / 6: Acylation;
DOI:10.1039/a904067f

Reference yield:

: 251643-16-0
methyl 2-(4-(methylamino)phenyl)acetate

: 251643-19-3
N-(N',N'-Dimethylaminoethyl)-4-[N-methyl-N-(tert-butyloxycarbonyl)amino]phenylacetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 62 percent / DMAP / tetrahydrofuran / 16 h / Heating

2: 97 percent / LiOH; H₂O / methanol / 0.5 h / 50 °C

3: dimethylformamide / 0.17 h / 50 °C

4: dimethylformamide / 2 h / 20 °C

With dmap; lithium hydroxide; water; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; 1: Substitution / 2: Hydrolysis / 3: Substitution / 4: Acylation;
DOI:10.1039/a904067f