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methyl 2-({5-chloro-2-[(phenylmethyl)oxy]phenyl}methyl)-1,3-thiazole-4-carboximidoate hydrochloride

Base Information Edit
  • Chemical Name:methyl 2-({5-chloro-2-[(phenylmethyl)oxy]phenyl}methyl)-1,3-thiazole-4-carboximidoate hydrochloride
  • CAS No.:913652-22-9
  • Molecular Formula:C19H17ClN2O2S*ClH
  • Molecular Weight:409.336
  • Hs Code.:
  • Mol file:913652-22-9.mol
methyl 2-({5-chloro-2-[(phenylmethyl)oxy]phenyl}methyl)-1,3-thiazole-4-carboximidoate hydrochloride

Synonyms:methyl 2-({5-chloro-2-[(phenylmethyl)oxy]phenyl}methyl)-1,3-thiazole-4-carboximidoate hydrochloride

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Chemical Property of methyl 2-({5-chloro-2-[(phenylmethyl)oxy]phenyl}methyl)-1,3-thiazole-4-carboximidoate hydrochloride Edit
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Technology Process of methyl 2-({5-chloro-2-[(phenylmethyl)oxy]phenyl}methyl)-1,3-thiazole-4-carboximidoate hydrochloride

There total 9 articles about methyl 2-({5-chloro-2-[(phenylmethyl)oxy]phenyl}methyl)-1,3-thiazole-4-carboximidoate 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:
methanol; 2-({5-chloro-2-[(phenylmethyl)oxy]phenyl}methyl)-1,3-thiazole-4-carbonitrile; With sodium hydride; at 20 ℃;
With hydrogenchloride; In diethyl ether;
Guidance literature:
Multi-step reaction with 10 steps
1.1: potassium carbonate / 2 h / Heating / reflux
2.1: iodine; silver nitrate / ethanol / 16 h / Heating / reflux
3.1: water / ethanol / 1.5 h / 90 °C
4.1: 4-methyl-morpholine; N-hydroxybenzotriazole ammonium salt; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide / dichloromethane / 2 h / 20 °C
5.1: Lawessons reagent / 1,2-dimethoxyethane / 2 h / 20 °C
6.1: potassium hydrogencarbonate / 1,2-dimethoxyethane / 0.08 h
6.2: 0.02 h
6.3: 1.5 h / 0 - 20 °C
7.1: sodium hydroxide; water / ethanol / 20 - 60 °C
8.1: 4-methyl-morpholine; N-hydroxybenzotriazole ammonium salt; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide / dichloromethane / 2 h / 20 °C
9.1: phosphorus (III) oxychloride / 1 h / 90 °C
10.1: sodium hydride / 20 °C
With Lawessons reagent; 4-methyl-morpholine; sodium hydroxide; N-hydroxybenzotriazole ammonium salt; phosphorus (III) oxychloride; water; iodine; sodium hydride; potassium carbonate; potassium hydrogencarbonate; silver nitrate; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In 1,2-dimethoxyethane; ethanol; dichloromethane;
Guidance literature:
Multi-step reaction with 3 steps
1: 4-methyl-morpholine; N-hydroxybenzotriazole ammonium salt; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide / dichloromethane / 2 h / 20 °C
2: phosphorus (III) oxychloride / 1 h / 90 °C
3: sodium hydride / 20 °C
With 4-methyl-morpholine; N-hydroxybenzotriazole ammonium salt; phosphorus (III) oxychloride; sodium hydride; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; In dichloromethane;
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