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Chemical Structure| 840493-96-1 Chemical Structure| 840493-96-1

Structure of 840493-96-1

Chemical Structure| 840493-96-1

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Product Details of [ 840493-96-1 ]

CAS No. :840493-96-1
Formula : C13H19BrN2O4S
M.W : 379.27
SMILES Code : O=C(OC(C)(C)C)N(C1=NC=C(Br)S1)C(OC(C)(C)C)=O

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Application In Synthesis of [ 840493-96-1 ]

* 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 [ 840493-96-1 ]

[ 840493-96-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24424-99-5 ]
  • [ 405939-39-1 ]
  • [ 840493-96-1 ]
YieldReaction ConditionsOperation in experiment
85% With dmap; triethylamine; In tetrahydrofuran; at 0 - 20℃; Di-tert-butyl dicarbonate [(Boc)20, 90.4 g, 0.414 mol, 1.2 eq] was added to a flask containing a mixture of intermediate lb? (97.9 g, 0.35 1 mol, 1.0 eq) and 4- (dimethylamino)pyridine (DMAP, 1.07 g, 8.7 mmol, 0.025 eq) in 880 ml of THF and 121 ml of Et3N and cooled to 0 C using an ice bath. The reaction mixture was stirred at rt overnight. Water (200 ml) and DCM were added and the resulting mixture was stirred at rt for 30 mm. The organic layer was separated and the aqueous layer was extracted with DCM (2 x 150 ml). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude residue was purified with a short silica gel column (eluting with EtOAc/Heptane 1:20) to give intermediate lc? as an off-white solid (113 g, 85% yield).
55% With dmap; In tetrahydrofuran; at 60℃; for 0.5h; To a solution of <strong>[405939-39-1]tert-butyl (5-bromothiazol-2-yl)carbamate</strong> (0.5 g, 1.79 mmol, 1.0 eq) in THF (20 mL) was added di-tert-butyl dicarbonate (0.39 g, 1.79 mmol, 1.0 eq) and DMAP (0.1 g, 0.9 mmol 0.5 eq). The resulting mixture was stirred at 60 C for 30 mm, cooled to room temperature, diluted with H20 (25 mL), and extracted with EtOAc (50 mL x2). The combined organic layers were dried, filtered, concentrated, and purified by prep-TLC to give compound 110-2 (0.35 g, 0.92 mmol, 55% yield). LCMS: RT = 0.944 mi m/z 379.0 [M+H] ?HNIVIR (CDC13, 400 IVIHz) 5 7.40 (s, 1H), 1.54 (s, 18H).
 

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