tert-butyl ((2R,3R)-2-(allyloxy)-4-(N-((2S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((2S)-pent-4-en-2-yloxy)nicotinamido)-3-methylbutyl)carbamate

Base Information

Chemical Name:tert-butyl ((2R,3R)-2-(allyloxy)-4-(N-((2S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((2S)-pent-4-en-2-yloxy)nicotinamido)-3-methylbutyl)carbamate
CAS No.:1403480-72-7
Molecular Formula:C₃₆H₅₃N₃O₇
Molecular Weight:639.833
Hs Code.:

Synonyms:tert-butyl ((2R,3R)-2-(allyloxy)-4-(N-((2S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((2S)-pent-4-en-2-yloxy)nicotinamido)-3-methylbutyl)carbamate

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Chemical Property of tert-butyl ((2R,3R)-2-(allyloxy)-4-(N-((2S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((2S)-pent-4-en-2-yloxy)nicotinamido)-3-methylbutyl)carbamate

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Technology Process of tert-butyl ((2R,3R)-2-(allyloxy)-4-(N-((2S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((2S)-pent-4-en-2-yloxy)nicotinamido)-3-methylbutyl)carbamate

There total 7 articles about tert-butyl ((2R,3R)-2-(allyloxy)-4-(N-((2S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((2S)-pent-4-en-2-yloxy)nicotinamido)-3-methylbutyl)carbamate 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:

: 1403480-54-5
tert-butyl ((2R,3R)-2-hydroxy-4-(N-((2S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((2S)-pent-4-en-2-yloxy)nicotinamido)-3-methylbutyl)carbamate

: 106-95-6
allyl bromide

: 1403480-72-7
tert-butyl ((2R,3R)-2-(allyloxy)-4-(N-((2S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((2S)-pent-4-en-2-yloxy)nicotinamido)-3-methylbutyl)carbamate

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0 - 20 ℃; for 16h;
DOI:10.1021/jm500994n

Reference yield:

: 625-31-0,64584-92-5,111957-98-3,55563-79-6
(S)-4-penten-2-ol

: 1403480-72-7
tert-butyl ((2R,3R)-2-(allyloxy)-4-(N-((2S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((2S)-pent-4-en-2-yloxy)nicotinamido)-3-methylbutyl)carbamate

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hexamethyldisilazane / tetrahydrofuran / 1.5 h / -8 - 20 °C

2: sodium hydroxide / isopropyl alcohol / 18 h

3: N-ethyl-N,N-diisopropylamine; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride / dichloromethane / 1.5 h / 0 - 20 °C

4: tetrabutyl ammonium fluoride / tetrahydrofuran / 16 h / 0 °C

5: sodium hydride / N,N-dimethyl-formamide; mineral oil / 16 h / 0 - 20 °C

With tetrabutyl ammonium fluoride; sodium hexamethyldisilazane; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; sodium hydride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol; mineral oil;
DOI:10.1021/jm500994n

Reference yield:

: 232951-83-6
tert-butyl 2-chloropyridine-3-carboxylate

: 1403480-72-7
tert-butyl ((2R,3R)-2-(allyloxy)-4-(N-((2S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-2-((2S)-pent-4-en-2-yloxy)nicotinamido)-3-methylbutyl)carbamate

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hexamethyldisilazane / tetrahydrofuran / 1.5 h / -8 - 20 °C

2: sodium hydroxide / isopropyl alcohol / 18 h

3: N-ethyl-N,N-diisopropylamine; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride / dichloromethane / 1.5 h / 0 - 20 °C

4: tetrabutyl ammonium fluoride / tetrahydrofuran / 16 h / 0 °C

5: sodium hydride / N,N-dimethyl-formamide; mineral oil / 16 h / 0 - 20 °C

With tetrabutyl ammonium fluoride; sodium hexamethyldisilazane; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; sodium hydride; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol; mineral oil;
DOI:10.1021/jm500994n