(2S,3R)-3-(1-{Benzyloxycarbonylamino-[(E)-benzyloxycarbonylimino]-methyl}-piperidin-3-ylmethyl)-4-oxo-azetidine-2-carboxylic acid benzyl ester

Base Information

Chemical Name:(2S,3R)-3-(1-{Benzyloxycarbonylamino-[(E)-benzyloxycarbonylimino]-methyl}-piperidin-3-ylmethyl)-4-oxo-azetidine-2-carboxylic acid benzyl ester
CAS No.:384830-18-6
Molecular Formula:C₃₄H₃₆N₄O₇
Molecular Weight:612.682
Hs Code.:

(2S,3R)-3-(1-{Benzyloxycarbonylamino-[(E)-benzyloxycarbonylimino]-methyl}-piperidin-3-ylmethyl)-4-oxo-azetidine-2-carboxylic acid benzyl ester

Synonyms:

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Chemical Property of (2S,3R)-3-(1-{Benzyloxycarbonylamino-[(E)-benzyloxycarbonylimino]-methyl}-piperidin-3-ylmethyl)-4-oxo-azetidine-2-carboxylic acid benzyl ester

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Technology Process of (2S,3R)-3-(1-{Benzyloxycarbonylamino-[(E)-benzyloxycarbonylimino]-methyl}-piperidin-3-ylmethyl)-4-oxo-azetidine-2-carboxylic acid benzyl ester

There total 10 articles about (2S,3R)-3-(1-{Benzyloxycarbonylamino-[(E)-benzyloxycarbonylimino]-methyl}-piperidin-3-ylmethyl)-4-oxo-azetidine-2-carboxylic acid benzyl 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:

: C₂HF₃O₂*C₁₇H₂₂N₂O₃

: 25508-20-7
N,N'-dibenzyloxycarbonyl-(S)-methyl-isothiourea

: 384830-18-6
(2S,3R)-3-(1-{Benzyloxycarbonylamino-[(E)-benzyloxycarbonylimino]-methyl}-piperidin-3-ylmethyl)-4-oxo-azetidine-2-carboxylic acid benzyl ester

Guidance literature:: With triethylamine; In DMF (N,N-dimethyl-formamide); at 0 - 20 ℃; for 20h;

Reference yield:

: 148672-74-6,130250-54-3
ethyl N-(t-butyloxycarbonyl)nipecotate

: 384830-18-6
(2S,3R)-3-(1-{Benzyloxycarbonylamino-[(E)-benzyloxycarbonylimino]-methyl}-piperidin-3-ylmethyl)-4-oxo-azetidine-2-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: LAH / tetrahydrofuran

2: I₂; PPh₃; imidazole / CH₂Cl₂

3: LDA / tetrahydrofuran

4: TBAF / tetrahydrofuran

5: NaHCO₃ / dimethylformamide

6: TFA / CH₂Cl₂

7: Hg(OAc)2; TEA / dimethylformamide

With 1H-imidazole; lithium aluminium tetrahydride; TEA; mercury(II) diacetate; tetrabutyl ammonium fluoride; iodine; sodium hydrogencarbonate; triphenylphosphine; trifluoroacetic acid; lithium diisopropyl amide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(02)00689-3

Reference yield:

: 116574-71-1
(±)-tert-butyl 3-(hydroxymethyl)piperidine-1-carboxylate

: 384830-18-6
(2S,3R)-3-(1-{Benzyloxycarbonylamino-[(E)-benzyloxycarbonylimino]-methyl}-piperidin-3-ylmethyl)-4-oxo-azetidine-2-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: I₂; PPh₃; imidazole / CH₂Cl₂

2: LDA / tetrahydrofuran

3: TBAF / tetrahydrofuran

4: NaHCO₃ / dimethylformamide

5: TFA / CH₂Cl₂

6: Hg(OAc)2; TEA / dimethylformamide

With 1H-imidazole; TEA; mercury(II) diacetate; tetrabutyl ammonium fluoride; iodine; sodium hydrogencarbonate; triphenylphosphine; trifluoroacetic acid; lithium diisopropyl amide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0960-894X(02)00689-3