D-6-benzyloxycarbonylamino-6-[N-(2′,4′-dimethoxybenzyl)carbamoyl]hexanoic acid ethyl ester

Base Information

Chemical Name:D-6-benzyloxycarbonylamino-6-[N-(2′,4′-dimethoxybenzyl)carbamoyl]hexanoic acid ethyl ester
CAS No.:1429301-61-0
Molecular Formula:C₂₆H₃₄N₂O₇
Molecular Weight:486.565
Hs Code.:

Synonyms:D-6-benzyloxycarbonylamino-6-[N-(2′,4′-dimethoxybenzyl)carbamoyl]hexanoic acid ethyl ester

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Chemical Property of D-6-benzyloxycarbonylamino-6-[N-(2′,4′-dimethoxybenzyl)carbamoyl]hexanoic acid ethyl ester

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Technology Process of D-6-benzyloxycarbonylamino-6-[N-(2′,4′-dimethoxybenzyl)carbamoyl]hexanoic acid ethyl ester

There total 3 articles about D-6-benzyloxycarbonylamino-6-[N-(2′,4′-dimethoxybenzyl)carbamoyl]hexanoic acid ethyl 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:

: 1429301-58-5
D-6-(N,N-dibenzylamino)-6-(benzyloxycarbonyl)-trans-hex-2-enoic acid ethyl ester

: 1429301-61-0
D-6-benzyloxycarbonylamino-6-[N-(2′,4′-dimethoxybenzyl)carbamoyl]hexanoic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: palladium 10% on activated carbon; hydrogen / methanol; ethyl acetate / 16 h / 20 °C / 2585.81 Torr

2.1: sodium carbonate / water; 1,4-dioxane / 20 °C

3.1: HATU / N,N-dimethyl-formamide / Inert atmosphere

3.2: 20 °C / Inert atmosphere; Cooling

With palladium 10% on activated carbon; hydrogen; sodium carbonate; HATU; In 1,4-dioxane; methanol; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/bi400211q

Reference yield:

: 1237770-00-1
D-4-(N,N-dibenzylamino)-4-(benzyloxycarbonyl)butanal

: 1429301-61-0
D-6-benzyloxycarbonylamino-6-[N-(2′,4′-dimethoxybenzyl)carbamoyl]hexanoic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrahydrofuran / 4 h / 20 °C / Inert atmosphere

2.1: palladium 10% on activated carbon; hydrogen / methanol; ethyl acetate / 16 h / 20 °C / 2585.81 Torr

3.1: sodium carbonate / water; 1,4-dioxane / 20 °C

4.1: HATU / N,N-dimethyl-formamide / Inert atmosphere

4.2: 20 °C / Inert atmosphere; Cooling

With palladium 10% on activated carbon; hydrogen; sodium carbonate; HATU; In tetrahydrofuran; 1,4-dioxane; methanol; water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/bi400211q

Reference yield:

: 1429301-59-6
D-α-aminopimelic acid ethyl ester

: 1429301-61-0
D-6-benzyloxycarbonylamino-6-[N-(2′,4′-dimethoxybenzyl)carbamoyl]hexanoic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium carbonate / water; 1,4-dioxane / 20 °C

2.1: HATU / N,N-dimethyl-formamide / Inert atmosphere

2.2: 20 °C / Inert atmosphere; Cooling

With sodium carbonate; HATU; In 1,4-dioxane; water; N,N-dimethyl-formamide;
DOI:10.1021/bi400211q