(S)-6-Imidazol-1-yl-6-oxo-5-(9-phenyl-9H-fluoren-9-ylamino)-hexanoic acid methyl ester

Base Information

Chemical Name:(S)-6-Imidazol-1-yl-6-oxo-5-(9-phenyl-9H-fluoren-9-ylamino)-hexanoic acid methyl ester
CAS No.:147698-08-6
Molecular Formula:C₂₉H₂₇N₃O₃
Molecular Weight:465.552
Hs Code.:

Synonyms:(S)-6-Imidazol-1-yl-6-oxo-5-(9-phenyl-9H-fluoren-9-ylamino)-hexanoic acid methyl ester

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Chemical Property of (S)-6-Imidazol-1-yl-6-oxo-5-(9-phenyl-9H-fluoren-9-ylamino)-hexanoic acid methyl ester

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Technology Process of (S)-6-Imidazol-1-yl-6-oxo-5-(9-phenyl-9H-fluoren-9-ylamino)-hexanoic acid methyl ester

There total 7 articles about (S)-6-Imidazol-1-yl-6-oxo-5-(9-phenyl-9H-fluoren-9-ylamino)-hexanoic 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: 97.0%

: 147698-07-5
(S)-2-hexanedioic acid γ-methyl ester

: 530-62-1
1,1'-carbonyldiimidazole

: 147698-08-6
(S)-6-Imidazol-1-yl-6-oxo-5-(9-phenyl-9H-fluoren-9-ylamino)-hexanoic acid methyl ester

Guidance literature:: In tetrahydrofuran; for 20h; Ambient temperature;
DOI:10.1021/jo00061a006

Reference yield:

: 147698-04-2
1-tert-Butyl 6-methyl (S)-2-hex-4-enedioate

: 147698-08-6
(S)-6-Imidazol-1-yl-6-oxo-5-(9-phenyl-9H-fluoren-9-ylamino)-hexanoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / H₂, HCl / 10percent Pd/C / ethyl acetate / a) 16 h, b) r.t., 24 h

2: 77 percent / propylene oxide / ethanol / 6 h / Heating

3: 1.) trimethylsilyl chloride, 2.) Et₃N, Pb(NO₃)2 / 1.) CH₂Cl₂, reflux, 2 h, 2.) CH₂Cl₂, r.t., 96 h

4: 97 percent / tetrahydrofuran / 20 h / Ambient temperature

With hydrogenchloride; chloro-trimethyl-silane; lead(II) nitrate; hydrogen; triethylamine; methyloxirane; palladium on activated charcoal; In tetrahydrofuran; ethanol; ethyl acetate;
DOI:10.1021/jo00061a006

Reference yield:

: 55135-66-5
9-bromo-9-phenyl-9H-fluorene

: 147698-08-6
(S)-6-Imidazol-1-yl-6-oxo-5-(9-phenyl-9H-fluoren-9-ylamino)-hexanoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / K₃PO₄ / nitromethane / 72 h / Ambient temperature

2: 89 percent / HCl / ethyl acetate / 24 h / Ambient temperature

3: 97 percent / tetrahydrofuran / 20 h / Ambient temperature

With hydrogenchloride; potassium phosphate; In tetrahydrofuran; nitromethane; ethyl acetate;
DOI:10.1021/jo00061a006