(R)-2-{2-[(R)-2-Amino-1-piperidin-1-yl-prop-(E)-ylideneamino]-benzoylamino}-3-(1H-indol-3-yl)-propionic acid methyl ester

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Chemical Name:(R)-2-{2-[(R)-2-Amino-1-piperidin-1-yl-prop-(E)-ylideneamino]-benzoylamino}-3-(1H-indol-3-yl)-propionic acid methyl ester
CAS No.:221552-09-6
Molecular Formula:C₂₇H₃₃N₅O₃
Molecular Weight:475.591
Hs Code.:

Synonyms:(R)-2-{2-[(R)-2-Amino-1-piperidin-1-yl-prop-(E)-ylideneamino]-benzoylamino}-3-(1H-indol-3-yl)-propionic acid methyl ester

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Chemical Property of (R)-2-{2-[(R)-2-Amino-1-piperidin-1-yl-prop-(E)-ylideneamino]-benzoylamino}-3-(1H-indol-3-yl)-propionic acid methyl ester

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Technology Process of (R)-2-{2-[(R)-2-Amino-1-piperidin-1-yl-prop-(E)-ylideneamino]-benzoylamino}-3-(1H-indol-3-yl)-propionic acid methyl ester

There total 2 articles about (R)-2-{2-[(R)-2-Amino-1-piperidin-1-yl-prop-(E)-ylideneamino]-benzoylamino}-3-(1H-indol-3-yl)-propionic 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: 93.0%

: 110-89-4
piperidine

: 221552-06-3
N-{2-[(R)-1-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-aminoethyl]-4H-3,1-benzoxazin-4-ylidene}-D-tryptophan methyl ester

: 221552-09-6
(R)-2-{2-[(R)-2-Amino-1-piperidin-1-yl-prop-(E)-ylideneamino]-benzoylamino}-3-(1H-indol-3-yl)-propionic acid methyl ester

Guidance literature:: In ethyl acetate; at 25 ℃; for 1h;
DOI:10.1021/jo9820465

Reference yield:

: 205042-95-1
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-alanyl-2-aminobenzoyl-D-tryptophan methyl ester

: 221552-09-6
(R)-2-{2-[(R)-2-Amino-1-piperidin-1-yl-prop-(E)-ylideneamino]-benzoylamino}-3-(1H-indol-3-yl)-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / PPh₃; I₂; EtN(i-Pr)2 / CH₂Cl₂ / 25 °C

2: 93 percent / ethyl acetate / 1 h / 25 °C

With iodine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In dichloromethane; ethyl acetate; 1: Cyclization / 2: Ring cleavage;
DOI:10.1021/jo9820465