(S)-4-Azidocarbonyl-2-{4-[(2,4-diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-butyric acid

Base Information

Chemical Name:(S)-4-Azidocarbonyl-2-{4-[(2,4-diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-butyric acid
CAS No.:121788-83-8
Molecular Formula:C₂₀H₂₁N₁₁O₄
Molecular Weight:479.458
Hs Code.:

Synonyms:(S)-4-Azidocarbonyl-2-{4-[(2,4-diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-butyric acid

Suppliers and Price of (S)-4-Azidocarbonyl-2-{4-[(2,4-diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-butyric acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (S)-4-Azidocarbonyl-2-{4-[(2,4-diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-butyric acid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-4-Azidocarbonyl-2-{4-[(2,4-diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-butyric acid

There total 5 articles about (S)-4-Azidocarbonyl-2-{4-[(2,4-diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-butyric 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:

Reference yield:

: 79640-75-8
N'-<4--N-methylamino>benzoyl>-L-glutamic acid γ-hydrazide

: 121788-83-8
(S)-4-Azidocarbonyl-2-{4-[(2,4-diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-butyric acid

Guidance literature:: With hydrogenchloride; tert.-butylnitrite; In tetrahydrofuran; N,N-dimethyl-formamide; at -20 ℃; for 1h;
DOI:10.1021/jm00131a003

Reference yield:

: 59-05-2
N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-L-glutamic acid

: 121788-83-8
(S)-4-Azidocarbonyl-2-{4-[(2,4-diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-butyric acid

Guidance literature:: Multi-step reaction with 3 steps

1: 73 percent / sodium sulfate / tetrafluoroboric acid etherate / 18 h / Ambient temperature

2: 91 percent / N₂H₄*H₂O / methanol / 48 h / Ambient temperature

3: tert-butyl nitrite, 2.4 M HCl / dimethylformamide; tetrahydrofuran / 1 h / -20 °C

With hydrogenchloride; tert.-butylnitrite; hydrazine hydrate; sodium sulfate; tetrafluoroboric acid diethyl ether; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00131a003

Reference yield:

: 10541-83-0,937737-33-2
N-methyl-p-aminobenzoic acid

: 121788-83-8
(S)-4-Azidocarbonyl-2-{4-[(2,4-diamino-pteridin-6-ylmethyl)-methyl-amino]-benzoylamino}-butyric acid

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) dibromotriphenylphosphorane, 2.) N-ethyldiisopropylamine / 1.) DMA, room temperature, 24 h, 2.) room temperature, 48 h

2: 1.) diethyl cyanophosphonate, N-ethyldiisopropylamine, 2.) N-ethyldiisopropylamine / 1.) DMF, room temperature, 4 h, 2.) room temperature, 72 h

3: 91 percent / N₂H₄*H₂O / methanol / 48 h / Ambient temperature

4: tert-butyl nitrite, 2.4 M HCl / dimethylformamide; tetrahydrofuran / 1 h / -20 °C

With hydrogenchloride; tert.-butylnitrite; diethyl cyanophosphonate; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; dibromotriphenylphosphorane; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1021/jm00131a003