benzyl (2S,5'S)-2-benzyloxycarbonylamino-3-(1-methyl-2,4-dioxo-3-phenylhexahydropyrimidin-5-yl)propionate

Base Information

Chemical Name:benzyl (2S,5'S)-2-benzyloxycarbonylamino-3-(1-methyl-2,4-dioxo-3-phenylhexahydropyrimidin-5-yl)propionate
CAS No.:326891-01-4
Molecular Formula:C₂₉H₂₉N₃O₆
Molecular Weight:515.566
Hs Code.:

Synonyms:benzyl (2S,5'S)-2-benzyloxycarbonylamino-3-(1-methyl-2,4-dioxo-3-phenylhexahydropyrimidin-5-yl)propionate

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Chemical Property of benzyl (2S,5'S)-2-benzyloxycarbonylamino-3-(1-methyl-2,4-dioxo-3-phenylhexahydropyrimidin-5-yl)propionate

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Technology Process of benzyl (2S,5'S)-2-benzyloxycarbonylamino-3-(1-methyl-2,4-dioxo-3-phenylhexahydropyrimidin-5-yl)propionate

There total 10 articles about benzyl (2S,5'S)-2-benzyloxycarbonylamino-3-(1-methyl-2,4-dioxo-3-phenylhexahydropyrimidin-5-yl)propionate 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: 20.0%

: 326890-99-7
benzyl (2S,4S)-N-benzyloxycarbonyl-4-[(1-methyl-3-phenylureido)methyl]pyroglutamate

: 326891-01-4
benzyl (2S,5'S)-2-benzyloxycarbonylamino-3-(1-methyl-2,4-dioxo-3-phenylhexahydropyrimidin-5-yl)propionate

Guidance literature:: at 130 ℃; for 111h;

Reference yield: 12.6%

: benzyl (2S)-N-benzyloxycarbonyl-4-[(1-methyl-3-phenylureido)methyl]pyroglutamate

: 326891-01-4
benzyl (2S,5'S)-2-benzyloxycarbonylamino-3-(1-methyl-2,4-dioxo-3-phenylhexahydropyrimidin-5-yl)propionate

: 326891-02-5
benzyl (2S,5'R)-2-benzyloxycarbonylamino-3-(1-methyl-2,4-dioxo-3-phenylhexahydropyrimidin-5-yl)propionate

Guidance literature:: With sodium hydride; In tetrahydrofuran; at 20 ℃; for 2h;

Reference yield:

: 326890-92-0
(E)-benzyl (2S)-N-benzyloxycarbonyl-4-N-methylaminomethylenepyroglutamate

: 326891-01-4
benzyl (2S,5'S)-2-benzyloxycarbonylamino-3-(1-methyl-2,4-dioxo-3-phenylhexahydropyrimidin-5-yl)propionate

Guidance literature:: Multi-step reaction with 3 steps

1: 99 percent / NaBH₄ / acetic acid / 0.42 h

2: CH₂Cl₂ / 15 h / 20 °C

3: 20 percent / 111 h / 130 °C

With sodium tetrahydroborate; In dichloromethane; acetic acid;