1-(4-N-benzoyl-2'-dideoxy-2',2'-difluoro-5'-iodo-β-D-ribofuranosyl)cytosine

Base Information

Chemical Name:1-(4-N-benzoyl-2'-dideoxy-2',2'-difluoro-5'-iodo-β-D-ribofuranosyl)cytosine
CAS No.:1145869-47-1
Molecular Formula:C₁₆H₁₄F₂IN₃O₄
Molecular Weight:477.206
Hs Code.:

Synonyms:1-(4-N-benzoyl-2'-dideoxy-2',2'-difluoro-5'-iodo-β-D-ribofuranosyl)cytosine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-(4-N-benzoyl-2'-dideoxy-2',2'-difluoro-5'-iodo-β-D-ribofuranosyl)cytosine

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Technology Process of 1-(4-N-benzoyl-2'-dideoxy-2',2'-difluoro-5'-iodo-β-D-ribofuranosyl)cytosine

There total 3 articles about 1-(4-N-benzoyl-2'-dideoxy-2',2'-difluoro-5'-iodo-β-D-ribofuranosyl)cytosine 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: 90.0%

: 142816-70-4
N⁴-benzoyl-2'-deoxy-2',2'-difluorocytidine

: 1145869-47-1
1-(4-N-benzoyl-2'-dideoxy-2',2'-difluoro-5'-iodo-β-D-ribofuranosyl)cytosine

Guidance literature:: With iodine; triphenylphosphine; In pyridine; acetonitrile; at 0 - 20 ℃;
DOI:10.1021/jm801595c

Reference yield:

: 122111-03-9
gemcitabine hydrochloride

: 1145869-47-1
1-(4-N-benzoyl-2'-dideoxy-2',2'-difluoro-5'-iodo-β-D-ribofuranosyl)cytosine

Guidance literature:: Multi-step reaction with 2 steps

1.1: pyridine; chloro-trimethyl-silane / 0.5 h / 0 - 20 °C

1.2: 0 - 20 °C

2.1: pyridine; triphenylphosphine; iodine / tetrahydrofuran / 60 h / 0 - 20 °C

With pyridine; chloro-trimethyl-silane; iodine; triphenylphosphine; In tetrahydrofuran;

Reference yield:

: 98-88-4
benzoyl chloride

: 1145869-47-1
1-(4-N-benzoyl-2'-dideoxy-2',2'-difluoro-5'-iodo-β-D-ribofuranosyl)cytosine

Guidance literature:: Multi-step reaction with 2 steps

1.1: pyridine; chloro-trimethyl-silane / 0.5 h / 0 - 20 °C

1.2: 0 - 20 °C

2.1: pyridine; triphenylphosphine; iodine / tetrahydrofuran / 60 h / 0 - 20 °C

With pyridine; chloro-trimethyl-silane; iodine; triphenylphosphine; In tetrahydrofuran;