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Chemical Structure| 745078-03-9

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Product Details of [ 745078-03-9 ]

CAS No. :745078-03-9
Formula : C10H14N2O4S
M.W : 258.29
SMILES Code : O=C(C1=CN=C(NC(OC(C)(C)C)=O)S1)OC
MDL No. :MFCD11655929

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Application In Synthesis of [ 745078-03-9 ]

* 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 [ 745078-03-9 ]

[ 745078-03-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 6633-61-0 ]
  • [ 24424-99-5 ]
  • [ 745078-03-9 ]
YieldReaction ConditionsOperation in experiment
100% With dmap; triethylamine; In tetrahydrofuran; at 20℃; for 16h; 2-Amino-thiazole-5-carboxylic acid methyl ester (4.0 g, 25.28 mmol) was suspended in THF (100 ml). Di-tert-butyl dicarbonate (6.63 g, 30.34 mmol) was added to the reaction vessel and the mixture was stirred vigorously. Next, Triethylamine (7.05 mL, 50.57 mmol) and 4-Dimethylaminopyridine (316 mg, 2.53 mmol) were added to the reaction. The reaction was stirred at room temperature for 16 hours. A brown precipitate was present upon completion of the reaction. The reaction mixture was concentrated down in vacuo and dried in a vacuum oven to afford the crude product, 2-tert-Butoxycarbonylamino-thiazole-5- carboxylic acid methyl ester (6.5 g, 100% yield), which was then taken on to subsequent reaction. LCMS [M+H] 258.9.
38% With triethylamine;dmap; In tetrahydrofuran; at 0 - 20℃; for 20h; A solution of di-tert-butyl dicarbonate (1.66 g; 7.59 mmol) in THF (10 mL) was added to a 0 C. solution of <strong>[6633-61-0]methyl 2-aminothiazole-5-carboxylate</strong> (1.20 g; 7.59 mmol) in THF (20 mL). TEA (1.11 mL; 7.97 mmol) was added followed by a catalytic amount of 4-DMAP (10 mg). The reaction mixture was then stirred at RT for 20 h, then was concentrated in vacuo. The residue was partitioned between EtOAc (80 mL) and 0.2 N aqueous HCl (40 mL). The organic phase was washed with brine (40 mL), dried (MgSO4) and concentrated in vacuo to give Part A compound (1.70 g; yield given below in Part B). The crude product was taken forward without further purification.
Intermediate 4[00176] A solution of di-tert-butyl dicarbonate (1.66 g; 7.59 mmol) in THF (10 mL) was added to a 0C solution of <strong>[6633-61-0]methyl 2-aminothiazole-5-carboxylate</strong> (1.20 g; 7.59 mmol) in THF (20 mL). TEA (1.1 1 mL; 7.97 mmol) was added followed by a catalytic amount of 4-DMAP (10 mg). The reaction mixture was then stirred at RT for 20 h, then was concentrated in vacuo. The residue was partitioned between EtOAc (80 mL) and 0.2 N aqueous HC1 (40 mL). The organic phase was washed with brine (40 mL), dried (MgS04) and concentrated in vacuo to give Part A compound (1.70 g; yield given below in Part B). The crude product was taken forward without further purification.
  • 2
  • [ 67-56-1 ]
  • [ 302964-20-1 ]
  • [ 745078-03-9 ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; [00106] Compound 8 was made using by adapfing the synthesisdsdosed n J.Med.Chem. 2006, 6819. Synthesis of amde 5 was accomphshedn two steps, starting from compound 1. Compound I was converted to acidchorde 2 using oxay chorde n dchoromethane (DCM). Formafion of theacd chorde was confirmed by quenching an aquot n methano (MeOH);LCMS anayss ndcated the presence of the corresponding methy? ester 3 n>90%. Add Won of 2 to a mixture of excess anWne 4 and dsopropy ethyamne(DPEA) gave good conversion to amine 5. After fHtehng the sohds off thisafforded 1.15 g (40%) amde 5 n high purIty. Remova of the Boc-group using tr[fluoroacefic acid (TFA) gave good conversion to amine 6. Amine 6 was converted to compound 8 n the presence of compound 7 and sodium t-butoxde (NaOBu-t).
 

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