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Chemical Structure| 23957-21-3 Chemical Structure| 23957-21-3

Structure of 23957-21-3

Chemical Structure| 23957-21-3

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Product Details of [ 23957-21-3 ]

CAS No. :23957-21-3
Formula : C8H10BrNO2
M.W : 232.07
SMILES Code : NC1=C(OC)C=C(Br)C=C1OC
MDL No. :MFCD09909335
InChI Key :UJGUWWZOHPAMAJ-UHFFFAOYSA-N
Pubchem ID :329423

Safety of [ 23957-21-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H317
Precautionary Statements:P264-P270-P301+P312-P330-P302+P352-P333+P313-P321-P261-P272-P280-P363-P501

Application In Synthesis of [ 23957-21-3 ]

* 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 [ 23957-21-3 ]

[ 23957-21-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2734-70-5 ]
  • [ 23957-21-3 ]
YieldReaction ConditionsOperation in experiment
79% With bromine; In chloroform; at 0 - 21℃; for 14h; This reaction was not performed under inert conditions.A solution of bromine (1.00 mL, 3.12 g, 1.95 mmol, 1.00 equiv) in chloroform (50 mL) was added to asolution of <strong>[2734-70-5]2,6-dimethoxyaniline</strong> (3.06 g, 2.00 mmol, 1.03 equiv) in chloroform (50 mL) at 0C over thecourse of 1 h. Afterwards, the solution was warmed up to 21 C and stirred for additional 14 h. Then,NaOH (2 M) was added to adjust the pH to 11. The water phase was extracted with ethyl acetate (3 ×100 mL). The combined organic phases were washed with water (100 mL), brine (100 mL), dried overMgSO4 and filtered. The crude product was purified by column chromatography (eluent: nhexane/DCM 95:5) to yield S4 as a colorless solid (3.66 g, 1.58 mmol, 79%, Lit.:[14] 77%)
70% With bromine; In dichloromethane; at 4 - 20℃; To a stirred solution of <strong>[2734-70-5]2,6-dimethoxyaniline</strong> (9.0 g, 58.7 mmol, 1.0 eq) in 350 mL of anhydrous DCM was dropwise added over 30 min a Br2solution in 50 mL of anhydrous DCM at 4 C. An additional 200 mL was added to the slurry to achieve a semi-homogeneous solution. The reaction mixture was stirred overnight at room temperature. The dark brown mixture was cooled to 4 C and basified by addition of 1.0 M NaOH solution (ca.100 mL) to pH = 10-11. The mixture was diluted with 200 mL of DCM and the layers are separated. The aqueous layer was extracted with DCM (200 mL total). The combined DCM layers were washed with water, brine, and dried over Na2SO4. After concentration in vacuo, the crude product was obtained as a slightly reddish solid. The residue was dissolved in DCM (8 mL) and loaded onto a 220 g HP silica gel Gold RediSep column and purified via ISCO (gradient elution: 5 - 95% EA in hexanes), pure fractions combined, and the solvent evaporated in vacuo. The solid was triturated with DCM and hexanes and filtered. The off-while solid was dried in vacuo giving the title compound R26 as an off-white230.99; found 231.9 and 234.0 (M+H).1H NMR (500 MHz; CDCl3) t 6.66 (s, 2H), 3.84 (s, 6H)
70% With bromine; In dichloromethane; at 4 - 20℃; To a stirred solution of <strong>[2734-70-5]2,6-dimethoxyaniline</strong> (9.0 g, 58.7 mmol, 1.0 eq) in 350 mL of anhydrous DCM was dropwise added over 30 min a Bn solution in 50 mL of anhydrous DCM at 4 C. An additional 200 mL was added to the slurry to achieve a semi-homogeneous solution. The reaction mixture was stirred overnight at room temperature. The dark brown mixture was cooled to 4 C and basified by addition of 1.0 M NaOH solution ( ca . 100 mL) to pH = 10-11. The mixture was diluted with 200 mL of DCM and the layers are separated. The aqueous layer was extracted with DCM (200 mL total). The combined DCM layers were washed with water, brine, and dried over NaiSCri. After concentration in vacuo , the crude product was obtained as a slightly reddish solid. The residue was dissolved in DCM (8 mL) and loaded onto a 220 g HP silica gel Gold RediSep column and purified via ISCO (gradient elution: 5 - 95% EA in hexanes), pure fractions combined, and the solvent evaporated in vacuo. The solid was triturated with DCM and hexanes and filtered. The off-while solid was dried in vacuo giving the title compound 26 as an off-white solid (9.4 g, 70%). MS (ESI, pos.): calc’d for CxHioBrNCb, 230.99; found 231.9 and 234.0 (M+H). ‘H NMR (500 MHz; CDCT) S 6.66 (s, 2H), 3.84 (s, 6H).
54.8% Example 10: [(2R,5R)-17,20-Dimethoxy-3,12-dioxo-2-(l-oxo-l,2-dihydro- isoquinolin-7-ylamino)-13-oxa-4,ll-diaza-tricyclo[14.2.2.1 ' jhenicosa- l(19),6,8,10(21),16(20),17-hexaen-5-yl]-acetic acid ethyl ester; <n="132"/>[00281] A solution of bromine (6.6 mL, 127 mmol) in CH2Cl2 (100 mL) was added dropwise to a solution of <strong>[2734-70-5]2,6-dimethoxyaniline</strong> (19.5 g, 127 mmol) in CH2Cl2 (1273 mL) at 0 0C over 5 h. The reaction mixture was stirred for an additional 30 min and then NaOH (1.0 M, 500 mL) was added. The phases were separated and the organic phase was washed with H2O (1x250 mL), brine (1x250 mL), dried over Na2SO4 and concentrated. The crude brown oil was purified by column chromatography (0 to 50% EtOAc in hexanes) to yield 1OA (20 g, 69.8 mmol, 54.8 % yield) as a white solid.

 

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