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4-Hydroxy-6-methyl-2-(3-nitro-pyridin-2-yl)-isophthalic acid 1-(4-diethylamino-but-2-ynyl) ester 3-methyl ester; hydrochloride

Base Information
  • Chemical Name:4-Hydroxy-6-methyl-2-(3-nitro-pyridin-2-yl)-isophthalic acid 1-(4-diethylamino-but-2-ynyl) ester 3-methyl ester; hydrochloride
  • CAS No.:142549-69-7
  • Molecular Formula:C23H25N3O7*ClH
  • Molecular Weight:491.928
  • Hs Code.:
4-Hydroxy-6-methyl-2-(3-nitro-pyridin-2-yl)-isophthalic acid 1-(4-diethylamino-but-2-ynyl) ester 3-methyl ester; hydrochloride

Synonyms:4-Hydroxy-6-methyl-2-(3-nitro-pyridin-2-yl)-isophthalic acid 1-(4-diethylamino-but-2-ynyl) ester 3-methyl ester; hydrochloride

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Chemical Property of 4-Hydroxy-6-methyl-2-(3-nitro-pyridin-2-yl)-isophthalic acid 1-(4-diethylamino-but-2-ynyl) ester 3-methyl ester; hydrochloride
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Technology Process of 4-Hydroxy-6-methyl-2-(3-nitro-pyridin-2-yl)-isophthalic acid 1-(4-diethylamino-but-2-ynyl) ester 3-methyl ester; hydrochloride

There total 6 articles about 4-Hydroxy-6-methyl-2-(3-nitro-pyridin-2-yl)-isophthalic acid 1-(4-diethylamino-but-2-ynyl) ester 3-methyl ester; hydrochloride 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:
Multi-step reaction with 6 steps
1: 100 percent / K2CO3 / dimethylformamide / 19 h / Ambient temperature
2: 98.4 percent / NaI, K2CO3 / dimethylformamide / 3 h
3: 63.1 percent / m-chloroperbenzoic acid / CHCl3 / 1 h
4: 83.7 percent / 1 N aq. NaOH / methanol; tetrahydrofuran / 0.5 h / Ambient temperature
5: 1.) NaH, 2.) Et3N / 1.) DMF, RT, 20 min, 2.) DMF, 100 deg C, 13 h
6: 98.4 percent / HCl / methanol; CHCl3 / 1.5 h / Heating
With hydrogenchloride; sodium hydroxide; sodium hydride; potassium carbonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; sodium iodide; In tetrahydrofuran; methanol; chloroform; N,N-dimethyl-formamide;
DOI:10.1248/cpb.40.899
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) NaH, 2.) Et3N / 1.) DMF, RT, 20 min, 2.) DMF, 100 deg C, 13 h
2: 98.4 percent / HCl / methanol; CHCl3 / 1.5 h / Heating
With hydrogenchloride; sodium hydride; triethylamine; In methanol; chloroform;
DOI:10.1248/cpb.40.899
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