2-[N¹-2-pyrimidinyl-p-(benzyloxycarbonylamino)benzenesulfonamido]ethanol

Base Information

• Chemical Name: 2-[N¹-2-pyrimidinyl-p-(benzyloxycarbonylamino)benzenesulfonamido]ethanol
• CAS No.: 288066-52-4
• Molecular Formula: C₂₀H₂₀N₄O₅S
• Molecular Weight: 428.469
• Mol file: 288066-52-4.mol

Synonyms:2-[N¹-2-pyrimidinyl-p-(benzyloxycarbonylamino)benzenesulfonamido]ethanol

Chemical Property of 2-[N¹-2-pyrimidinyl-p-(benzyloxycarbonylamino)benzenesulfonamido]ethanol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
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MSDS Files:

Useful:

Technology Process of 2-[N¹-2-pyrimidinyl-p-(benzyloxycarbonylamino)benzenesulfonamido]ethanol

There total 4 articles about 2-[N¹-2-pyrimidinyl-p-(benzyloxycarbonylamino)benzenesulfonamido]ethanol 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: 43.0%

2-bromoethanol (540-51-2) + C18H15N4O4S(1-)*Na(1+) → 2-[N1-2-pyrimidinyl-p-(benzyloxycarbonylamino)benzenesulfonamido]ethanol (288066-52-4)

Guidance literature:

In N,N-dimethyl-formamide; at 80 ℃; for 8h;

DOI:10.1016/S0223-5234(01)01285-5

Reference yield:

2-bromoethanol (540-51-2) + N1-2-pyrimidyl-p-(benzyloxycarbonylamino)benzenesulfonamide (288066-50-2) → 2-[N1-2-pyrimidinyl-p-(benzyloxycarbonylamino)benzenesulfonamido]ethanol (288066-52-4)

Guidance literature:

N¹-2-pyrimidyl-p-(benzyloxycarbonylamino)benzenesulfonamide; With sodium hydroxide;

2-bromoethanol; In N,N-dimethyl-formamide; at 80 ℃; for 8h;

DOI:10.1016/S0960-894X(01)00157-3

Reference yield:

sulfadiazine (68-35-9) → 2-[N1-2-pyrimidinyl-p-(benzyloxycarbonylamino)benzenesulfonamido]ethanol (288066-52-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 17.3 g / pyridine / 8 h / 20 °C

2: 43 percent / dimethylformamide / 8 h / 80 °C

In pyridine; N,N-dimethyl-formamide;

DOI:10.1016/S0223-5234(01)01285-5

upstream raw materials:

2-bromoethanol

N¹-2-pyrimidyl-p-(benzyloxycarbonylamino)benzenesulfonamide

sulfadiazine

benzyl chloroformate

Downstream raw materials:

4-{4-[bis-(2-chloro-ethyl)-amino]-phenyl}-butyric acid 2-[(4-benzyloxycarbonylamino-benzenesulfonyl)-pyrimidin-2-yl-amino]-ethyl ester