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tert-butyl 3-(2-acrylamido-5-(4-(2-(3-hydroxyphenyl)-4-morpholinothieno[3,2-d]pyrimidin-6-yl)-1,2,3,6-tetrahydropyridine-1-carbonyl)phenoxy)propylcarbamate

Base Information
  • Chemical Name:tert-butyl 3-(2-acrylamido-5-(4-(2-(3-hydroxyphenyl)-4-morpholinothieno[3,2-d]pyrimidin-6-yl)-1,2,3,6-tetrahydropyridine-1-carbonyl)phenoxy)propylcarbamate
  • CAS No.:1276109-92-2
  • Molecular Formula:C39H44N6O7S
  • Molecular Weight:740.88
  • Hs Code.:
tert-butyl 3-(2-acrylamido-5-(4-(2-(3-hydroxyphenyl)-4-morpholinothieno[3,2-d]pyrimidin-6-yl)-1,2,3,6-tetrahydropyridine-1-carbonyl)phenoxy)propylcarbamate

Synonyms:tert-butyl 3-(2-acrylamido-5-(4-(2-(3-hydroxyphenyl)-4-morpholinothieno[3,2-d]pyrimidin-6-yl)-1,2,3,6-tetrahydropyridine-1-carbonyl)phenoxy)propylcarbamate

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Chemical Property of tert-butyl 3-(2-acrylamido-5-(4-(2-(3-hydroxyphenyl)-4-morpholinothieno[3,2-d]pyrimidin-6-yl)-1,2,3,6-tetrahydropyridine-1-carbonyl)phenoxy)propylcarbamate
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Technology Process of tert-butyl 3-(2-acrylamido-5-(4-(2-(3-hydroxyphenyl)-4-morpholinothieno[3,2-d]pyrimidin-6-yl)-1,2,3,6-tetrahydropyridine-1-carbonyl)phenoxy)propylcarbamate

There total 11 articles about tert-butyl 3-(2-acrylamido-5-(4-(2-(3-hydroxyphenyl)-4-morpholinothieno[3,2-d]pyrimidin-6-yl)-1,2,3,6-tetrahydropyridine-1-carbonyl)phenoxy)propylcarbamate 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 5 steps
1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 1 h / 20 °C / Inert atmosphere
2: hydrogen / palladium 10% on activated carbon / methanol
3: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.25 h / -20 °C
4: sodium hydroxide; water / 1,4-dioxane / 20 °C
5: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl acetamide
With di-isopropyl azodicarboxylate; water; hydrogen; N-ethyl-N,N-diisopropylamine; triphenylphosphine; HATU; sodium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl acetamide; 1: Mitsunobu reaction;
Guidance literature:
Multi-step reaction with 5 steps
1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 1 h / 20 °C / Inert atmosphere
2: hydrogen / palladium 10% on activated carbon / methanol
3: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.25 h / -20 °C
4: sodium hydroxide; water / 1,4-dioxane / 20 °C
5: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl acetamide
With di-isopropyl azodicarboxylate; water; hydrogen; N-ethyl-N,N-diisopropylamine; triphenylphosphine; HATU; sodium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl acetamide; 1: Mitsunobu reaction;
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