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methyl Nα-{1-[(2,4-diaminopteridin-6-yl)methyl]indolin-5-ylcarbonyl}-Nδ-(3-ethoxycarbonylphenyl)-L-glutaminate

Base Information
  • Chemical Name:methyl Nα-{1-[(2,4-diaminopteridin-6-yl)methyl]indolin-5-ylcarbonyl}-Nδ-(3-ethoxycarbonylphenyl)-L-glutaminate
  • CAS No.:142166-28-7
  • Molecular Formula:C31H33N9O6
  • Molecular Weight:627.66
  • Hs Code.:
methyl N<sup>α</sup>-{1-[(2,4-diaminopteridin-6-yl)methyl]indolin-5-ylcarbonyl}-N<sup>δ</sup>-(3-ethoxycarbonylphenyl)-L-glutaminate

Synonyms:methyl Nα-{1-[(2,4-diaminopteridin-6-yl)methyl]indolin-5-ylcarbonyl}-Nδ-(3-ethoxycarbonylphenyl)-L-glutaminate

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Chemical Property of methyl Nα-{1-[(2,4-diaminopteridin-6-yl)methyl]indolin-5-ylcarbonyl}-Nδ-(3-ethoxycarbonylphenyl)-L-glutaminate
Chemical Property:
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Technology Process of methyl Nα-{1-[(2,4-diaminopteridin-6-yl)methyl]indolin-5-ylcarbonyl}-Nδ-(3-ethoxycarbonylphenyl)-L-glutaminate

There total 8 articles about methyl Nα-{1-[(2,4-diaminopteridin-6-yl)methyl]indolin-5-ylcarbonyl}-Nδ-(3-ethoxycarbonylphenyl)-L-glutaminate 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: 69 percent / 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC) / CH2Cl2 / Ambient temperature
2: 88 percent / TFA / 0.5 h / Ambient temperature
3: aq. K2CO3 / CH2Cl2 / 10 h / Ambient temperature
4: H2 / 5percent Pd/C / methanol / Ambient temperature
5: N,N-dimethyl-acetamide / 6 h / 55 °C
With hydrogen; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl acetamide;
DOI:10.1248/cpb.45.1146
Guidance literature:
Multi-step reaction with 5 steps
1: 69 percent / 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC) / CH2Cl2 / Ambient temperature
2: 88 percent / TFA / 0.5 h / Ambient temperature
3: aq. K2CO3 / CH2Cl2 / 10 h / Ambient temperature
4: H2 / 5percent Pd/C / methanol / Ambient temperature
5: N,N-dimethyl-acetamide / 6 h / 55 °C
With hydrogen; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl acetamide;
DOI:10.1248/cpb.45.1146
Guidance literature:
Multi-step reaction with 3 steps
1: aq. K2CO3 / CH2Cl2 / 10 h / Ambient temperature
2: H2 / 5percent Pd/C / methanol / Ambient temperature
3: N,N-dimethyl-acetamide / 6 h / 55 °C
With hydrogen; potassium carbonate; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl acetamide;
DOI:10.1248/cpb.45.1146
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