(2-{7-[6-tert-butoxycarbonylamino-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-2-oxo-2H-chromen-4-yl}-acetylamino)-acetic acid benzyl ester

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Chemical Name:(2-{7-[6-tert-butoxycarbonylamino-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-2-oxo-2H-chromen-4-yl}-acetylamino)-acetic acid benzyl ester
CAS No.:525579-02-6
Molecular Formula:C₄₆H₄₈N₄O₁₀
Molecular Weight:816.908
Hs Code.:

(2-{7-[6-<i>tert</i>-butoxycarbonylamino-2-(9<i>H</i>-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-2-oxo-2<i>H</i>-chromen-4-yl}-acetylamino)-acetic acid benzyl ester

Synonyms:(2-{7-[6-tert-butoxycarbonylamino-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-2-oxo-2H-chromen-4-yl}-acetylamino)-acetic acid benzyl ester

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Chemical Property of (2-{7-[6-tert-butoxycarbonylamino-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-2-oxo-2H-chromen-4-yl}-acetylamino)-acetic acid benzyl ester

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Technology Process of (2-{7-[6-tert-butoxycarbonylamino-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-2-oxo-2H-chromen-4-yl}-acetylamino)-acetic acid benzyl ester

There total 3 articles about (2-{7-[6-tert-butoxycarbonylamino-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-2-oxo-2H-chromen-4-yl}-acetylamino)-acetic 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: 45.0%

: 71989-26-9
Fmoc-Lys(tert-butoxycarbonyl)

: 141692-66-2
benzyl 7-aminocoumarin-4-acetamidoacetate

: 525579-02-6
(2-{7-[6-tert-butoxycarbonylamino-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-2-oxo-2H-chromen-4-yl}-acetylamino)-acetic acid benzyl ester

Guidance literature:: With 2,3,5-trimethyl-pyridine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 20 ℃; for 72h;
DOI:10.1021/ol034233h

Reference yield:

: 1738-68-7
Gly-OBz

: 525579-02-6
(2-{7-[6-tert-butoxycarbonylamino-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-2-oxo-2H-chromen-4-yl}-acetylamino)-acetic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / DIEA; DMAP; EDC / dimethylformamide / 20 °C

2: 45 percent / HATU; collidine / dimethylformamide / 72 h / 20 °C

With 2,3,5-trimethyl-pyridine; dmap; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide;
DOI:10.1021/ol034233h

Reference yield:

: 85157-21-7
2-(7-amino-2-oxo-2H-chromen-4-yl)acetic acid

: 525579-02-6
(2-{7-[6-tert-butoxycarbonylamino-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoylamino]-2-oxo-2H-chromen-4-yl}-acetylamino)-acetic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / DIEA; DMAP; EDC / dimethylformamide / 20 °C

2: 45 percent / HATU; collidine / dimethylformamide / 72 h / 20 °C

With 2,3,5-trimethyl-pyridine; dmap; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide;
DOI:10.1021/ol034233h