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[ CAS No. 1022151-47-8 ] {[proInfo.proName]}

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Chemical Structure| 1022151-47-8
Chemical Structure| 1022151-47-8
Structure of 1022151-47-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1022151-47-8 ]

CAS No. :1022151-47-8 MDL No. :MFCD19687231
Formula : C11H8BrNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :ZXPMRDCMTBPCLA-UHFFFAOYSA-N
M.W : 266.09 Pubchem ID :68530047
Synonyms :

Safety of [ 1022151-47-8 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P264-P270-P301+P312-P330 UN#:N/A
Hazard Statements:H302 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1022151-47-8 ]

* 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.

  • Upstream synthesis route of [ 1022151-47-8 ]
  • Downstream synthetic route of [ 1022151-47-8 ]

[ 1022151-47-8 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 1022151-47-8 ]
  • [ 13669-57-3 ]
YieldReaction ConditionsOperation in experiment
86% With methanol; potassium carbonate In water at 20℃; for 2 h; A solution of J.ii (1 g, 3.76 mmol) and K2C03 (1.04 g, 7.52 mmol) in MeOH/H20 (5 mL/3 mL) was stirred at rt for 2 hours. The reaction mixture was concentrated under reduced pressure to afford a crude solid which was further purified by washing with water, dried under vaccum to give the title compound J.iii as white solid (760 mg, yield 86percent). LCMS (method B): [M+H]+ = 224, tR = 2.29 min
86% With water; potassium carbonate In methanol at 20℃; for 2 h; A solution of Intermediate A (1 g, 3.76 mmol) and K2C03 (1.04 g, 7.52 mmol) in MeOH/H20 (5 mL/3 ml.) was stirred at rt for 2 hours. The reaction mixture was concentrated under reduced pressure to afford a crude solid which was further purified by washing with water, dried under vaccum to give the title compound as white solid (760 mg, yield 86percent). LCMS (method N): [M+H]+ = 224, tR = 2.29 min.
86% With water; potassium carbonate In methanol at 20℃; for 1 h; A solution of Intermediate A (1 g, 3.76 mmol) and K2CO3 (1.04 g, 7.52 mmol) in MeOH/H2O (5 mL/3 mL) was stirred at rt for 2 hours. The reaction mixture was concentrated under reduced pressure to afford a crude solid which was further purified by washing with water, dried under vacuum to give the title compound as white solid (760 mg, yield 86percent). LCMS (method N): [M+H]+=224, tR=2.29 min.
86% With potassium carbonate In methanol; water at 20℃; for 2 h; A solution of J.ii (1 g, 3.76 mmol) and K2CO3 (1.04 g, 7.52 mmol) in MeOH/H2O (5 mL/3 mL) was stirred at rt for 2 hours. The reaction mixture was concentrated under reduced pressure to afford a crude solid which was further purified by washing with water, dried under vacuum to give the title compound J.iii as white solid (760 mg, yield 86percent). LCMS (method B): [M+H]+=224, tR=2.29 min.

Reference: [1] Patent: WO2012/107500, 2012, A1, . Location in patent: Page/Page column 63; 64
[2] Patent: WO2013/38362, 2013, A1, . Location in patent: Page/Page column 75
[3] Patent: US2013/245002, 2013, A1, . Location in patent: Paragraph 0702
[4] Patent: US2013/324526, 2013, A1, . Location in patent: Paragraph 0456; 0459
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