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Chemical Structure| 94284-80-7 Chemical Structure| 94284-80-7

Structure of 94284-80-7

Chemical Structure| 94284-80-7

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Product Details of [ 94284-80-7 ]

CAS No. :94284-80-7
Formula : C6H8Br2N2OS
M.W : 316.01
SMILES Code : BrCC(C1=C(C)N=C(N)S1)=O.[H]Br
MDL No. :MFCD26398509

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Application In Synthesis of [ 94284-80-7 ]

* 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 [ 94284-80-7 ]

[ 94284-80-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 30748-47-1 ]
  • [ 94284-80-7 ]
YieldReaction ConditionsOperation in experiment
74% With hydrogen bromide; bromine; In 1,4-dioxane; water; at 60℃; for 3h; 5-Acetyl-2-amino-4-methylthiazole (P5) (1.0 g, 6.4 mmol) is suspended in 48% HBr solution in water (20 mL, 6.4 mmol). The mixture is warmed to 60 C and a solution of Br2 (0.262 mL, 5.12 mmol, 0.8 eq) in dioxane (20 mL) is added dropwise. The mixture is stirred at 60 C for 3 hours. The progression of the reaction is followed by LC/MS. When it is complete, the solvents are evaporated, and the water is removed by azeotropic distillation with toluene. The resulting solid is recrystallized in isopropanol/Et20 mixture, affording Intermediate 2 as colorless solid (890 mg, 74% yield).'H NMR (DMSO-d6) 8 : 2.46 (s, 3H), 4.50 (s, 3H), 6.90 (br s, 1H), 9.18 (br s, 2H). M- (ESI) : 234.1 ; M+ (ESI) : 236. 1.
74% With hydrogen bromide; bromine; In 1,4-dioxane; water; at 60℃; for 3h; 5-Acetyl-2-amino-4-methylthiazole (P5) (Flrochem) (1.0 g, 6.4 mmol) is suspended in 48% HBr solution in water (20 ml, 6.4 mmol). The mixture is warmed to 600C and a solution of Br2 (0.262 ml, 5.12 mmol, 0.8 eq.) in dioxane (20 ml) is added dropwise. The mixture is stirred at 600C for 3 hours. The progression of the reaction is followed by LC/MS. When it is complete, the solvents are evaporated, and the water is removed by azeotropic distillation with toluene. The resulting solid is recrystallized in isopropanol/Et2O mixture, affording Intermediate 2 as colorless solid (890 mg, 74% yield). It is used in bis-thiazol synthesis as HBr salt or as parent, after 5 min treatment with Amberlyst A21 in DCM/MeOH mixture. 1K NMR (DMSO-d6) δ: 2.46 (s, 3H), 4.50 (s, 3H), 6.90 (br s, IH), 9.18 (br s, 2H). M (ESI): 234.1; M+(ESI): 236.1.
47% With hydrogen bromide; phenyltrimethylammonium tribromide; acetic acid; at 20℃; A solution of <strong>[30748-47-1]5-acetyl-2-amino-4-methylthiazole</strong> (0.101 g, 0.599 mmol) and phenyltrimethylammonium tribromide (0.246 g, 0.658 mmol) in 33% of HBr in acetic acid was stirred at room temperature for overnight. The solution was poured into ice water and CH2Cl2. The undissolved solid was collected from the organic layer and washed with diethyl ether to give 1-(2-amino-4-methyl-1,3-thiazol-5-yl)-2-bromoethanone hydrobromide (0.680 g, 47%) as a white solid. 1H NMR (DMSO-d6, 300 MHz) δ 8.90-8.40 (br, 2H), 4.53 (s, 2H), 2.46 (s, 3H).
With hydrogen bromide; pyridinium hydrobromide perbromide; In acetic acid; EXAMPLE 44 To a suspension of 2-amino-4-methyl-5-acetylthiazole (15.6 g) in 30% solution of hydrogen bromide in acetic acid (120 ml) was added pyridinium hydrobromide perbromide (36 g) at ambient temperature and the mixture was stirred at the same temperature for 5 hours. The precipitate was collected by filtration, washed with diisopropyl ether, and dried over calcium chloride to give 2-amino-4-methyl-5-(2-bromoacetyl)thiazole hydrobromide (26.8 g). IR (Nujol): 1660, 1620, 1600, 1540 cm-1

 

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