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N-(4-{[(2,4-diaminopyrido[3,2-d]pyrimidin-6-yl)methyl]sulfanyl}benzoyl)glutamic acid

Base Information Edit
  • Chemical Name:N-(4-{[(2,4-diaminopyrido[3,2-d]pyrimidin-6-yl)methyl]sulfanyl}benzoyl)glutamic acid
  • CAS No.:76822-63-4
  • Molecular Formula:C20H20N6O5S
  • Molecular Weight:456.475
  • Hs Code.:
  • Mol file:76822-63-4.mol
N-(4-{[(2,4-diaminopyrido[3,2-d]pyrimidin-6-yl)methyl]sulfanyl}benzoyl)glutamic acid

Synonyms:

Suppliers and Price of N-(4-{[(2,4-diaminopyrido[3,2-d]pyrimidin-6-yl)methyl]sulfanyl}benzoyl)glutamic acid
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 2 raw suppliers
Chemical Property of N-(4-{[(2,4-diaminopyrido[3,2-d]pyrimidin-6-yl)methyl]sulfanyl}benzoyl)glutamic acid Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • Density:1.57g/cm3 
Purity/Quality:

99%min *data from raw suppliers

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Technology Process of N-(4-{[(2,4-diaminopyrido[3,2-d]pyrimidin-6-yl)methyl]sulfanyl}benzoyl)glutamic acid

There total 8 articles about N-(4-{[(2,4-diaminopyrido[3,2-d]pyrimidin-6-yl)methyl]sulfanyl}benzoyl)glutamic acid 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:
With sodium hydroxide; In ethanol; for 48h; Ambient temperature;
DOI:10.1021/jo00322a004
Guidance literature:
Multi-step reaction with 7 steps
1: 83 percent / m-Chloroperoxybenzoic acid / acetic acid / 3 h / Heating
2: 85 percent / acetic acid / 0.5 h / Heating
3: 62 percent / POCl3, (C2H5)3N / 8 h / Heating
4: 84 percent / liquid NH3 / 18 h / 160 - 170 °C
5: PBr3 / tetrahydrofuran / 8 h
6: 1.) NaBH4 / 1.) ethanol, 2.) dimethylacetamide, room temperature, 6 h
7: 68 percent / 1 N NaOH / ethanol / 48 h / Ambient temperature
With sodium hydroxide; sodium tetrahydroborate; ammonia; phosphorus tribromide; triethylamine; 3-chloro-benzenecarboperoxoic acid; trichlorophosphate; In tetrahydrofuran; ethanol; acetic acid;
DOI:10.1021/jo00322a004
Guidance literature:
Multi-step reaction with 6 steps
1: 85 percent / acetic acid / 0.5 h / Heating
2: 62 percent / POCl3, (C2H5)3N / 8 h / Heating
3: 84 percent / liquid NH3 / 18 h / 160 - 170 °C
4: PBr3 / tetrahydrofuran / 8 h
5: 1.) NaBH4 / 1.) ethanol, 2.) dimethylacetamide, room temperature, 6 h
6: 68 percent / 1 N NaOH / ethanol / 48 h / Ambient temperature
With sodium hydroxide; sodium tetrahydroborate; ammonia; phosphorus tribromide; triethylamine; trichlorophosphate; In tetrahydrofuran; ethanol; acetic acid;
DOI:10.1021/jo00322a004
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