(3S,4S)-4-p-(2,6-dichlorobenzyloxy)benzyl-1-p-methoxybenzyl-3-methyl-4-[2-(piperidin-1-yl)ethyl]carbamoyl-2-azetidinone

Base Information

Chemical Name:(3S,4S)-4-p-(2,6-dichlorobenzyloxy)benzyl-1-p-methoxybenzyl-3-methyl-4-[2-(piperidin-1-yl)ethyl]carbamoyl-2-azetidinone
CAS No.:1342306-05-1
Molecular Formula:C₃₄H₃₉Cl₂N₃O₄
Molecular Weight:624.607
Hs Code.:

Synonyms:(3S,4S)-4-p-(2,6-dichlorobenzyloxy)benzyl-1-p-methoxybenzyl-3-methyl-4-[2-(piperidin-1-yl)ethyl]carbamoyl-2-azetidinone

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Chemical Property of (3S,4S)-4-p-(2,6-dichlorobenzyloxy)benzyl-1-p-methoxybenzyl-3-methyl-4-[2-(piperidin-1-yl)ethyl]carbamoyl-2-azetidinone

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Technology Process of (3S,4S)-4-p-(2,6-dichlorobenzyloxy)benzyl-1-p-methoxybenzyl-3-methyl-4-[2-(piperidin-1-yl)ethyl]carbamoyl-2-azetidinone

There total 6 articles about (3S,4S)-4-p-(2,6-dichlorobenzyloxy)benzyl-1-p-methoxybenzyl-3-methyl-4-[2-(piperidin-1-yl)ethyl]carbamoyl-2-azetidinone 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: 71.0%

: 27578-60-5
1-(2-aminoethyl)piperidine

: 1342305-99-0
(3S,4S)-4-carboxy-4-p-(2,6-dichlorobenzyloxy)benzyl-1-p-methoxybenzyl-3-methyl-2-azetidinone

: 1342306-05-1
(3S,4S)-4-p-(2,6-dichlorobenzyloxy)benzyl-1-p-methoxybenzyl-3-methyl-4-[2-(piperidin-1-yl)ethyl]carbamoyl-2-azetidinone

Guidance literature:: With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1016/j.ejmech.2011.08.025

Reference yield:

: 1342305-95-6
N-[(S)-2-chloropropionyl]-N-p-methoxybenzyl-L-Tyr(2,6-dichlorobenzyl)-OMe

: 1342306-05-1
(3S,4S)-4-p-(2,6-dichlorobenzyloxy)benzyl-1-p-methoxybenzyl-3-methyl-4-[2-(piperidin-1-yl)ethyl]carbamoyl-2-azetidinone

Guidance literature:: Multi-step reaction with 3 steps

1.1: tert-butylimino-tri(pyrrolidino)phosphorane / acetonitrile / 20 °C

2.1: sodium hydroxide / methanol / 20 °C

2.2: pH 3

3.1: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine / dichloromethane / 12 h / 20 °C

With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; tert-butylimino-tri(pyrrolidino)phosphorane; sodium hydroxide; In methanol; dichloromethane; acetonitrile;
DOI:10.1016/j.ejmech.2011.08.025

Reference yield:

: 1342305-97-8
(3S,4S)-4-p-(2,6-dichlorobenzyloxy)benzyl-1-p-methoxybenzyl-4-methoxycarbonyl-3-methyl-2-azetidinone

: 1342306-05-1
(3S,4S)-4-p-(2,6-dichlorobenzyloxy)benzyl-1-p-methoxybenzyl-3-methyl-4-[2-(piperidin-1-yl)ethyl]carbamoyl-2-azetidinone

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydroxide / methanol / 20 °C

1.2: pH 3

2.1: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine / dichloromethane / 12 h / 20 °C

With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; sodium hydroxide; In methanol; dichloromethane;
DOI:10.1016/j.ejmech.2011.08.025