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ChemicalBook CAS DataBase List NSP-SA-NHS
199293-83-9

NSP-SA-NHS synthesis

5synthesis methods
6066-82-6 Synthesis
N-Hydroxysuccinimide

6066-82-6
745 suppliers
$5.00/10g

211106-69-3 Synthesis
3-[9-(((3-(carboxypropyl)[4-Methxylphenyl]sulfonyl)aMine)carboxyl]-10-acridiniuMyl)-1-propanesulfonate inner salt

211106-69-3
55 suppliers
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NSP-SA-NHS

199293-83-9
93 suppliers
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Yield:199293-83-9 92%

Reaction Conditions:

with 1,1'-carbonyldiimidazole in acetonitrile at 20; for 8 h;Inert atmosphere;Solvent;

Steps:

1; 1 Example 1:

See the chemical reaction formula shown in Figure 1,From 10-(3-sulfopropyl)-N-p-toluenesulfonyl-N-(3-carboxypropyl) acridine-9-carboxamide,That is, the compound of formula C prepares 9-[[[4-[(2,5-dioxo-1-pyrrolidinyl)oxy]-4-oxobutyl][(4-methylphenyl)sulfonyl ]Amino]carbonyl]-10-(3-sulfopropyl)-acridine internal salt,Formula D compound: after dissolving 200 mg of compound C with acetonitrile,The reaction solution was not dissolved, and 150 mg of N,N'-carbonyldiimidazole was added.After being ventilated by N2, wrapped in foil paper, activated at room temperature for 2h, the reaction solution gradually dissolved,Add 194 mg of N-hydroxysuccinimide and react at room temperature for 6h.A yellow solid precipitated, HPLC tracking showed that the raw material reaction was complete,Add 6 times the volume of acetonitrile tert-butyl methyl ether and stir to crystallize, suction filter, the filter cake was washed with a small amount of tert-butyl methyl ether, the solid was collected and suction dried213 mg of yellow solid was obtained, HPLC>98%, yield: 92%, stored at -20°C under shading.

References:

CN111170994,2020,A Location in patent:Paragraph 0023-0025

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