(S)-2-(Benzyl-methyl-amino)-3-(1-trityl-1H-imidazol-4-yl)-propionic acid methyl ester

Base Information

Chemical Name:(S)-2-(Benzyl-methyl-amino)-3-(1-trityl-1H-imidazol-4-yl)-propionic acid methyl ester
CAS No.:176752-36-6
Molecular Formula:C₃₄H₃₃N₃O₂
Molecular Weight:515.655
Hs Code.:

Synonyms:(S)-2-(Benzyl-methyl-amino)-3-(1-trityl-1H-imidazol-4-yl)-propionic acid methyl ester

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Chemical Property of (S)-2-(Benzyl-methyl-amino)-3-(1-trityl-1H-imidazol-4-yl)-propionic acid methyl ester

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Technology Process of (S)-2-(Benzyl-methyl-amino)-3-(1-trityl-1H-imidazol-4-yl)-propionic acid methyl ester

There total 8 articles about (S)-2-(Benzyl-methyl-amino)-3-(1-trityl-1H-imidazol-4-yl)-propionic acid methyl 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: 61.0%

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 176752-35-5
methyl (2S)-2-(benzylamino)-3-[1-(triphenylmethyl)-1H-imidazol-4-yl]propanoate

: 176752-36-6
(S)-2-(Benzyl-methyl-amino)-3-(1-trityl-1H-imidazol-4-yl)-propionic acid methyl ester

Guidance literature:: With sodium cyanoborohydride; acetic acid; In acetonitrile; at 25 ℃; for 0.333333h;
DOI:10.1016/0968-0896(95)00183-2

Reference yield:

: 76-83-5
trityl chloride

: 176752-36-6
(S)-2-(Benzyl-methyl-amino)-3-(1-trityl-1H-imidazol-4-yl)-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 99 percent / Et₃N / benzene / 1 h / 80 °C

2: 0.78 g / H₂ / 10percent Pd/C / methanol / 2.5 h / 25 °C / 760 Torr

3: methanol / 1.5 h / 25 °C

4: NaBH₄ / methanol / 0.5 h / 5 - 10 °C

5: 61 percent / NaBH₃CN, aq. AcOH / acetonitrile / 0.33 h / 25 °C

With sodium tetrahydroborate; hydrogen; sodium cyanoborohydride; acetic acid; triethylamine; palladium on activated charcoal; In methanol; acetonitrile; benzene;
DOI:10.1016/0968-0896(95)00183-2

Reference yield:

: 40917-50-8
1,N^α-bis-benzyloxycarbonyl-histidine methyl ester

: 176752-36-6
(S)-2-(Benzyl-methyl-amino)-3-(1-trityl-1H-imidazol-4-yl)-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 80 percent / 1N aq. NaOH / methanol / 0.01 h / -20 °C

2: 99 percent / Et₃N / benzene / 1 h / 80 °C

3: 0.78 g / H₂ / 10percent Pd/C / methanol / 2.5 h / 25 °C / 760 Torr

4: methanol / 1.5 h / 25 °C

5: NaBH₄ / methanol / 0.5 h / 5 - 10 °C

6: 61 percent / NaBH₃CN, aq. AcOH / acetonitrile / 0.33 h / 25 °C

With sodium hydroxide; sodium tetrahydroborate; hydrogen; sodium cyanoborohydride; acetic acid; triethylamine; palladium on activated charcoal; In methanol; acetonitrile; benzene;
DOI:10.1016/0968-0896(95)00183-2