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Chemical Structure| 1585234-56-5 Chemical Structure| 1585234-56-5

Structure of 1585234-56-5

Chemical Structure| 1585234-56-5

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Product Details of [ 1585234-56-5 ]

CAS No. :1585234-56-5
Formula : C24H28BrNO4
M.W : 474.39
SMILES Code : O=C1NC2=C(C([C@@H](OC(OCCCC)C)CBr)=CC=C2OCC3=CC=CC=C3)C=C1

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Application In Synthesis of [ 1585234-56-5 ]

* 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 [ 1585234-56-5 ]

[ 1585234-56-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 530084-79-8 ]
  • [ 111-34-2 ]
  • [ 1585234-56-5 ]
YieldReaction ConditionsOperation in experiment
100% With toluene-4-sulfonic acid; In tetrahydrofuran; toluene; at 20 - 25℃; for 0.5h;Molecular sieve; A flask was charged with 5 ml of tetrahydrofuran (THF) and 5 ml of toluene, p- toluene sulfonic acid (0,15 mmol) and molecular sieves were added with stirring for 30 minutes. 6 mmol of butyl-vinylether and 3 mmol of 8-(phenylmethoxy)-5- (( ?)-2-bromo-l-hydroxy-ethyl)-(l Y)-quinolin-2-one were added. The mixture was agitated at 20/25 C until completion of the reaction, followed by filtration and distillation of the filtrate to remove the solvent. The product is obtained in quantitative yield as an oil consisting of 50% of each of the diastereomers. 1H-NMR (DMSO-d6, delta), mixture 50/50 of diastereomers: 0.61 and 0.82 (3H, t, J=7.2 Hz, CH3-Pr-0), 1.12 and 1.22 (3H, d, J=5.6 Hz, acetalic CH3), 0.90-1.40 (4H, m, CH2 + CH2), 3.20-3.80 (4H, m, CH2-OAr + CH2-Br), 4.51 and 4.82 (1H, q, J=5.6 Hz, acetalic CH), 5.18 and 5.24 (1H, dd, J=4.0, 8.0 Hz, CH-O-acetal), 6.56 and 6.58 (1H, d, J = 10.0 Hz, H4), 7.00-7.57 (7H, m), 8.17 and 8.23 (1H, d, J = 10.0 Hz, H3), 10.71 (1H, s, NH) 13C-NMR (DMSO-c/6, delta), mixture 50/50 of diastereoisomers: 13.5 and 13.7 CH3), 18.5 and 18.8 (CH2), 19.9 and 20.0 (acetalic CH3), 30.9 and 31.4 (CH2), 36.8 and 37.3 (CH2), 63.7 and 64.2 (CH2-Br), 69.8 and 69.9 (CH2-OAr), 73.8 and 75.1 (CH- O), 97.5 and 100.4 (acetalic CH), 111.8 (CH), 116.9 and 117.2 (C), 121.2 and 122.4 (CH), 122.3 and 122.6 (CH), 127.7 and 127.8 (C), 127.8 and 127.9 (CH), 128.2 and 128.3 (CH), 128.8 and 129.1 (C), 129.4 and 129.6 (C), 136.1 and 136.5 (CH), 136.5 and 136.6 (C), 144.0 and 144.2 (C), 160.7 and 160.8 (C=0).
100% With toluene-4-sulfonic acid; In tetrahydrofuran; toluene; at 20 - 25℃; for 0.5h;Molecular sieve; A flask is charged with 5 ml of tetrahydrofuran (THF) and 5 ml of toluene, p- toluene sulfonic acid (0,15 mmol) and molecular sieves are added with stirring for 30 minutes. 6 mmol of butyl-vinylether and 3 mmol of 8-(phenylmethoxy)-5-((R)- 2-bromo-l-hydroxy-ethyl)-(lH)-quinolin-2-one are added. The mixture is agitated at 20/25 C until completion of the reaction, followed by filtration and distillation of the filtrate to remove the solvent. The product is obtained in quantitative yield as an oil consisting of 50% of each of the diastereomers. ^-NMR (DMSO-c/6, delta), mixture 50/50 of diastereomers: 0.61 and 0.82 (3H, t, J=7.2 Hz, CHs-Pr-O), 1.12 and 1.22 (3H, d, J=5.6 Hz, acetalic CH3), 0.90-1.40 (4H, m, CH2 + CH2), 3.20-3.80 (4H, m, CH2-OAr + CH2-Br), 4.51 and 4.82 (1H, q, J = 5.6 Hz, acetalic CH), 5.18 and 5.24 (1H, dd, J=4.0, 8.0 Hz, CH-O-acetal), 6.56 and 6.58 (1H, d, J = 10.0 Hz, H4), 7.00-7.57 (7H, m), 8.17 and 8.23 (1H, d, J = 10.0 Hz, H3), 10.71 (1H, s, NH) 13C-NMR (DMSO-c/6, delta), mixture 50/50 of diastereoisomers: 13.5 and 13.7 CH3), 18.5 and 18.8 (CH2), 19.9 and 20.0 (acetalic CH3), 30.9 and 31.4 (CH2), 36.8 and 37.3 (CH2), 63.7 and 64.2 (CH2-Br), 69.8 and 69.9 (CH2-OAr), 73.8 and 75.1 (CH- O), 97.5 and 100.4 (acetalic CH), 111.8 (CH), 116.9 and 117.2 (C), 121.2 and 122.4 (CH), 122.3 and 122.6 (CH), 127.7 and 127.8 (C), 127.8 and 127.9 (CH), 128.2 and 128.3 (CH), 128.8 and 129.1 (C), 129.4 and 129.6 (C), 136.1 and 136.5 (CH), 136.5 and 136.6 (C), 144.0 and 144.2 (C), 160.7 and 160.8 (C=0).
 

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