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N4-p-bromobenzoylcytidine

Base Information Edit
  • Chemical Name:N4-p-bromobenzoylcytidine
  • CAS No.:1386977-58-7
  • Molecular Formula:C16H16BrN3O6
  • Molecular Weight:426.224
  • Hs Code.:
  • Mol file:1386977-58-7.mol
N<sub>4</sub>-p-bromobenzoylcytidine

Synonyms:N4-p-bromobenzoylcytidine

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Chemical Property of N4-p-bromobenzoylcytidine Edit
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Technology Process of N4-p-bromobenzoylcytidine

There total 1 articles about N4-p-bromobenzoylcytidine 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:
Guidance literature:
CYTIDINE; With pyridine; chloro-trimethyl-silane; at 20 ℃; for 2h;
4-chlorobenzoyl chloride; for 2h;
With ammonia; In water; at 0 ℃; for 0.5h;
DOI:10.1021/ol301769j
Guidance literature:
N4-p-bromobenzoylcytidine; acetone; With perchloric acid; at 20 ℃; for 1.5h;
With ammonia; In water; for 0.25h;
DOI:10.1021/ol301769j
Guidance literature:
Multi-step reaction with 3 steps
1.1: perchloric acid / 1.5 h / 20 °C
1.2: 0.25 h
2.1: di-isopropyl azodicarboxylate; triphenylphosphine / dichloromethane / 3 h / 0 - 20 °C / Inert atmosphere
3.1: 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride / tetrahydrofuran / 0.75 h / 0 °C
With perchloric acid; di-isopropyl azodicarboxylate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triphenylphosphine; lithium chloride; In tetrahydrofuran; dichloromethane; 2.1: Mitsunobu reaction;
DOI:10.1021/ol301769j
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