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Chemical Structure| 1177325-80-2 Chemical Structure| 1177325-80-2

Structure of 1177325-80-2

Chemical Structure| 1177325-80-2

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Product Details of [ 1177325-80-2 ]

CAS No. :1177325-80-2
Formula : C10H9BrN2S
M.W : 269.16
SMILES Code : BrC1=CC=C2N=C(NC3CC3)SC2=C1
MDL No. :MFCD16653213

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Application In Synthesis of [ 1177325-80-2 ]

* 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 [ 1177325-80-2 ]

[ 1177325-80-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 408328-13-2 ]
  • [ 765-30-0 ]
  • [ 1177325-80-2 ]
YieldReaction ConditionsOperation in experiment
68% In 1,4-dioxane; for 6h;Inert atmosphere; <strong>[408328-13-2]2,6-dibromobenzo[d]thiazole</strong> (1.0 g, 3.4 mmol) was suspended in 1,4-dioxane (10 ml), and added cyclopropylamine (3.6 ml, 51.0 mmol). The resultant mixture is stirred under nitrogen for 6 hours and cool to room temperature. On completion of reaction following a TLC examination, the reaction mixture was extracted with ethyl acetate and washed with brine. The solvent was removed. The crude product obtained was purified by flash chromatography (Hex:AcOEt 1:1) to afford 6-bromo-N-cyclopropylbenzo[d]thiazol-2-amine (0.630 mg, 68 % yield) as pale yellow solid. MS: 268.97 [M++1].
56% In 1,4-dioxane; at 80℃; for 12h; General procedure: A mixture of <strong>[408328-13-2]2,6-dibromobenzo[d]thiazole</strong> (293 mg, 1.00 mmol) and corresponding amine (3 eq) in1,4-dioxane (3 mL) was heated to 80 C overnight. After cooling to room temperature, the solvent was removed by vacuum and the resulting residue was dissolved in ethyl acetate (50 mL), and washed with brine (10 mL * 3). The organic layer was dried over Na2SO4, and concentrated in vacuum to give the desired product.
0.44 g In 1,4-dioxane; for 6h;Inert atmosphere; Reflux; Compound 7a (1.0 g, 3.4 mmol) was suspended in 1,4-dioxane (10 ml), and cyclopropylamine (3.6 ml, 51.0 mmol) was added. The resulting mixture was heated to reflux under nitrogen for 6 h, cooled to room temperature. The solvent was evaporated off to give crude product which was purified through column chromatograph to give 8a (0.44 g, 48%) as off-white solid. Mp: 183.0-184.0 C; 1H NMR (DMSO-d6): δ 8.49 (s, 1H, NH), 7.97 (d, J = 2.0 Hz, 1H, Ar-H), 7.37 (d, J = 8.8 Hz, 1H, Ar-H), 7.33 (m, 1H, Ar-H), 2.68 (m, 1H, CH), 0.77 (m, 2H, CH2), 0.57 (m, 2H, CH2). ESI-HRMS m/z: calcd for C10H10BrN2S [M+H]+: 268.9748; found 268.9749.
 

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