(4S,5R)-1-((2R,3S)-1-Acetyl-3-methyl-aziridine-2-carbonyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one

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Chemical Name:(4S,5R)-1-((2R,3S)-1-Acetyl-3-methyl-aziridine-2-carbonyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one
CAS No.:176791-96-1
Molecular Formula:C₁₇H₂₁N₃O₃
Molecular Weight:315.372
Hs Code.:

Synonyms:(4S,5R)-1-((2R,3S)-1-Acetyl-3-methyl-aziridine-2-carbonyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one

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Chemical Property of (4S,5R)-1-((2R,3S)-1-Acetyl-3-methyl-aziridine-2-carbonyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one

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Technology Process of (4S,5R)-1-((2R,3S)-1-Acetyl-3-methyl-aziridine-2-carbonyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one

There total 6 articles about (4S,5R)-1-((2R,3S)-1-Acetyl-3-methyl-aziridine-2-carbonyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one 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: 91.0%

: 108-24-7
acetic anhydride

: 176791-95-0
(4R,5S)-1,5-Dimethyl-3-((2R,3S)-3-methyl-aziridine-2-carbonyl)-4-phenyl-imidazolidin-2-one

: 176791-96-1
(4S,5R)-1-((2R,3S)-1-Acetyl-3-methyl-aziridine-2-carbonyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one

Guidance literature:: With pyridine; dmap; In dichloromethane; at 0 ℃; for 2h;
DOI:10.1016/0957-4166(96)00071-7

Reference yield:

: 92841-65-1
(4R,5S)-1,5-dimethyl-4-phenylimidazolidin-2-one

: 176791-96-1
(4S,5R)-1-((2R,3S)-1-Acetyl-3-methyl-aziridine-2-carbonyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) CH₃MgCl / 1.) THF, 0 deg C, 20 min, 2.) THF, 3 h

2: 84 percent / NH₃ (gas) / dimethylsulfoxide / 1 h / Ambient temperature

3: 91 percent / pyridine, DMAP / CH₂Cl₂ / 2 h / 0 °C

With pyridine; dmap; ammonia; methylmagnesium chloride; In dichloromethane; dimethyl sulfoxide;
DOI:10.1016/0957-4166(96)00071-7

Reference yield:

: 139962-44-0
(4S,5R)-1-((E)-Hex-2-enoyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one

: 176791-96-1
(4S,5R)-1-((2R,3S)-1-Acetyl-3-methyl-aziridine-2-carbonyl)-3,4-dimethyl-5-phenyl-imidazolidin-2-one

Guidance literature:: Multi-step reaction with 6 steps

1: Br₂, CuBr₂ / CH₂Cl₂ / 6 h / -70 °C

2: 75 percent / NH₃ (gas) / dimethylsulfoxide / 2.5 h / Ambient temperature

3: 1.) BuLi / 1.) THF, -10 deg C, 20 min, 2.) THF, -10 deg C, 30 min

4: 1.) CH₃MgCl / 1.) THF, 0 deg C, 20 min, 2.) THF, 3 h

5: 84 percent / NH₃ (gas) / dimethylsulfoxide / 1 h / Ambient temperature

6: 91 percent / pyridine, DMAP / CH₂Cl₂ / 2 h / 0 °C

With pyridine; dmap; n-butyllithium; ammonia; bromine; methylmagnesium chloride; copper(ll) bromide; In dichloromethane; dimethyl sulfoxide;
DOI:10.1016/0957-4166(96)00071-7