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Chemical Structure| 680622-68-8 Chemical Structure| 680622-68-8

Structure of 680622-68-8

Chemical Structure| 680622-68-8

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Product Details of [ 680622-68-8 ]

CAS No. :680622-68-8
Formula : C10H15ClN6
M.W : 254.72
SMILES Code : C[N+]1(C2=C3NC=NC3=NC(N)=N2)CCCC1.[Cl-]
MDL No. :MFCD09753517

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Application In Synthesis of [ 680622-68-8 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 680622-68-8 ]

[ 680622-68-8 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 680622-68-8 ]
  • [ 171723-95-8 ]
  • [ 680622-70-2 ]
YieldReaction ConditionsOperation in experiment
69% With potassium tert-butylate; In N,N-dimethyl-formamide; at 25℃; for 3.0h;Inert atmosphere; A solution of 1.77 g of 4-[(trifluoroacetamido)methyl]benzyl alcohol (7.65 mmol) prepared in step (2) was dissolved in 15 mL of N, N-dimethylformamide, 900 mg of 1-(2-amino-9H-purin-6-yl)-1-methylpyrrolidinium chloride (3.54 mmol) prepared in step (1) and 1.8 g of potassium t-butoxide (16.1 mmol),The reaction was stirred at 25 C for 3 hours under argon. At the end of the reaction, an excess of potassium t-butoxide was added to the solution at pH 7 after which the mixture was extracted with methylene chloride and water (the volume ratio of dichloromethane to water was 1: 1). The methylene chloride layer was washed with Washed twice with water and dried in vacuo to give crude O-6-[4-trifluoroacetamidomethylbenzyl]guanine. The crude product was purified by column chromatography on silica gel eluting with methanol / methylene chloride gradient elution. The methanol / dichloromethane volume ratio was gradually changed from 1:50 to 1:10. O-6-[4-trifluoroacetamidomethylbenzyl]guanine (900 mg, 2.46 mmol) was obtained in 69% yield.
With sodium hydride; In N,N-dimethyl-formamide; at 20℃; for 3.0h; Reactive benzylguanine was produced by combining 2,2,2-Trifluoro-N-(4- hydroxymethyl-benzyl)- acetamide (2 in Fig. 2) with l-(2-Amino-7H-purin-6-yl)-l-methyl- pyrrolidinium chloride (1 in Fig. 2) in DMF to form N-[4-(2-Amino-9H-purin-6- yloxymethyl)-benzyl] 2,2,2-trifluoro-acetamide (3 in Fig. 2). Following that, in order to improve the synthesis and allow variability in the side chain used to extract these complexes, the dimethoxynitro benzyl photochemical protecting group was installed. Reagent (3 in Fig. 2) was treated with 3,4-dimethoxy-6-nitro-benzylbromide (4 in Fig. 2) in order to produce a 2: 1 mixture of the N9 (5 in Fig. 2) and N7 isomers (6 in Fig. 2) that were easily separable by flash column chromatography. Separating the isomers at this point prevents having to use HPLC purification during the last step of the synthesis, which makes it much easier to produce larger amounts of these compounds.
 

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