(Z)-3-[(2R,3R,4R,5S)-1-Benzyl-3,4-bis-benzyloxy-5-(4-methoxy-phenoxymethyl)-pyrrolidin-2-yl]-2-benzyloxycarbonylamino-acrylic acid methyl ester

Base Information

Chemical Name:(Z)-3-[(2R,3R,4R,5S)-1-Benzyl-3,4-bis-benzyloxy-5-(4-methoxy-phenoxymethyl)-pyrrolidin-2-yl]-2-benzyloxycarbonylamino-acrylic acid methyl ester
CAS No.:656832-21-2
Molecular Formula:C₄₅H₄₆N₂O₈
Molecular Weight:742.869
Hs Code.:

(Z)-3-[(2R,3R,4R,5S)-1-Benzyl-3,4-bis-benzyloxy-5-(4-methoxy-phenoxymethyl)-pyrrolidin-2-yl]-2-benzyloxycarbonylamino-acrylic acid methyl ester

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Chemical Property of (Z)-3-[(2R,3R,4R,5S)-1-Benzyl-3,4-bis-benzyloxy-5-(4-methoxy-phenoxymethyl)-pyrrolidin-2-yl]-2-benzyloxycarbonylamino-acrylic acid methyl ester

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Technology Process of (Z)-3-[(2R,3R,4R,5S)-1-Benzyl-3,4-bis-benzyloxy-5-(4-methoxy-phenoxymethyl)-pyrrolidin-2-yl]-2-benzyloxycarbonylamino-acrylic acid methyl ester

There total 6 articles about (Z)-3-[(2R,3R,4R,5S)-1-Benzyl-3,4-bis-benzyloxy-5-(4-methoxy-phenoxymethyl)-pyrrolidin-2-yl]-2-benzyloxycarbonylamino-acrylic acid methyl 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: 81.0%

: 100945-15-1,88568-95-0
N-(benzyloxycarbonyl)phosphonoglycine trimethyl ester

: 656832-19-8
(2S,3R,4R,5S)-1-Benzyl-3,4-bis-benzyloxy-5-(4-methoxy-phenoxymethyl)-pyrrolidine-2-carbaldehyde

: 656832-21-2
(Z)-3-[(2R,3R,4R,5S)-1-Benzyl-3,4-bis-benzyloxy-5-(4-methoxy-phenoxymethyl)-pyrrolidin-2-yl]-2-benzyloxycarbonylamino-acrylic acid methyl ester

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene;
DOI:10.1055/s-2003-43341

Reference yield:

: 260789-58-0
(2S,3R,4R,5S)-N-benzyl-3,4-dibenzyloxy-5-benzyloxymethyl-2-(1,3-thiazol-2-yl)pyrrolidine

: 656832-21-2
(Z)-3-[(2R,3R,4R,5S)-1-Benzyl-3,4-bis-benzyloxy-5-(4-methoxy-phenoxymethyl)-pyrrolidin-2-yl]-2-benzyloxycarbonylamino-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: H₂SO₄

2.1: NaOMe / methanol

3.1: 80 percent / PPh₃; DIAD

4.1: MeOTf

4.2: NaBH₄

4.3: 84 percent / aq. AgNO₃

5.1: 81 percent / DBU

With di-isopropyl azodicarboxylate; sulfuric acid; sodium methylate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triphenylphosphine; methyl trifluoromethanesulfonate; In methanol; 3.1: Mitsunobu reaction / 5.1: Horner-Emmons olefination;
DOI:10.1055/s-2003-43341

Reference yield:

: Acetic acid (2S,3R,4R,5S)-1-benzyl-3,4-bis-benzyloxy-5-thiazol-2-yl-pyrrolidin-2-ylmethyl ester

: 656832-21-2
(Z)-3-[(2R,3R,4R,5S)-1-Benzyl-3,4-bis-benzyloxy-5-(4-methoxy-phenoxymethyl)-pyrrolidin-2-yl]-2-benzyloxycarbonylamino-acrylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: NaOMe / methanol

2.1: 80 percent / PPh₃; DIAD

3.1: MeOTf

3.2: NaBH₄

3.3: 84 percent / aq. AgNO₃

4.1: 81 percent / DBU

With di-isopropyl azodicarboxylate; sodium methylate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triphenylphosphine; methyl trifluoromethanesulfonate; In methanol; 2.1: Mitsunobu reaction / 4.1: Horner-Emmons olefination;
DOI:10.1055/s-2003-43341