{[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid

Base Information

Chemical Name:{[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid
CAS No.:399564-52-4
Molecular Formula:C₃₈H₃₃N₅O₈
Molecular Weight:687.709
Hs Code.:

{[(4-benzyloxycarbonylamino-2-oxo-2<i>H</i>-pyrimidin-1-yl)-acetyl]-[2-(9<i>H</i>-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid

Synonyms:{[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid

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Chemical Property of {[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid

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Technology Process of {[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid

There total 1 articles about {[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid 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: 98.0%

: 399564-61-5
{[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid tert-butyl ester

: 399564-52-4
{[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃;
DOI:10.1021/ol010231q

Reference yield: 70.0%

: 399564-92-2
{(2-amino-benzyl)-[(6-benzyloxycarbonylamino-purin-9-yl)-acetyl]-amino}-acetic acid tert-butyl ester

: 399564-52-4
{[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid

: 399564-98-8
{[2-(2-{[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetylamino)-benzyl]-[(6-benzyloxycarbonylamino-purin-9-yl)-acetyl]-amino}-acetic acid tert-butyl ester

Guidance literature:: With 2,4,6-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 0 - 20 ℃;
DOI:10.1021/ol010231q

Reference yield:

: 399564-52-4
{[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetic acid

: {[2-(2-{[(4-benzyloxycarbonylamino-2-oxo-2H-pyrimidin-1-yl)-acetyl]-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-benzyl]-amino}-acetylamino)-benzyl]-[(6-benzyloxycarbonylamino-purin-9-yl)-acetyl]-amino}-acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / HATU; 2,4,6-collidine / dimethylformamide / 0 - 20 °C

2: 99 percent / TFA / CH₂Cl₂ / 20 °C

With 2,4,6-trimethyl-pyridine; trifluoroacetic acid; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ol010231q