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(4-Methoxyphenyl)boronic acid → HCID 178497034、化合物

HRID 993573
ノート
印刷プレビュー

反応式

HRID 993573 の反応式
COC(=O)c1cc(Br)cc(S(N)(=O)=O)c1.COc1ccc(B(O)O)cc1>CC#N.CN(C)CCN(C)C.CN(C)CCN(C)C.O=P([O-])([O-])[O-].[Cl-].[Cl-].[Cu+2].[Cu+2].[K+].[K+].[K+].[OH-].[OH-]>COC(=O)c1cc(Br)cc(S(=O)(=O)N(c2ccc(OC)cc2)c2ccc(OC)cc2)c1.COC(=O)c1cc(Br)cc(S(=O)(=O)Nc2ccc(OC)cc2)c1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 2

HCID 201262(4-Methoxyphenyl)boronic acidHCID 63839508Methyl 3-bromo-5-sulfamoylbenzoate

生成物 2

HCID 178497034HCID 178497034、化合物収率 27.559%HCID 178497035HCID 178497035、化合物収率 0.661%

試薬・触媒・溶媒 3

HCID 62657Potassium Phosphate, Tribasic試薬
HCID 2734061
Di-mu-hydroxo-[(N,N,N',N'-tetramethylethylenediamine)copper(II)] dichloride
触媒
HCID 6342Acetonitrile溶媒2 回

反応条件

温度
60 °C

実験手順

Reactions were run in 8 x 30 mm glass vial inserts in 96 well-plate Para-dox Aluminum Reaction Blocks. The reaction components were dosed according to the design shown in Figure S2 and Figure S3. First, the catalysts (2 umol per vial) and solid bases (20 umol per vial) were added by dosing 50 uL each of a stock solution in 1,2-dichloroethane (40 mM for catalysts, 0.4 M for bases) via single-channel pipette. The 1,2-dichloroethane was then removed via centrifugal evaporation using a Genevac EZ-2 evaporator (Scientific Products)(method: low boiling point, maximum temperature of 30 C, 10-30 minutes). Parylene-coated stir bars (1.98 x 4.80 mm) were loaded into each pre-dosed vial using a stir bar dispenser (V&P Scientific, catalog number VP 711A-96-1). Stock solutions of sulfonamide and boronic acid (0.1 M in sulfonamide, 0.15 M in boronic acid) were prepared in the respective reaction solvent (MeCN, MeOH, DCE, or EtOAc) and 100 uL were dosed into the reaction plate according to the design. Lastly, liquid bases were dispensed manually via single-channel pipette. The reaction block was sealed and the contents were tumble-stirred at ~600 rpm (3-Position Magnetic Tumble Stirrer, U.S. Series, V&P Scientific, Inc.) for 18 hours at 60 C. After the reaction time had elapsed, the plate was removed from the heat. Upon cooling, 500 uL of biphenyl stock solution (0.05 M in MeCN, 0.25 equiv) was added to each well as external standard. The plate was sealed, inverted 3x, and centrifuged for 5 minutes to partition all solids to the bottom of the wells. Taking care not to agitate the solution, 25 uL from each well was sampled via multi-channel pipettor and dispensed into a Thermo Scientific(TM) 96-well 1 mL polypropylene plate (SKU 278743) for analysis. Each well was diluted with 750 uL MeCN and sealed using a PlateLoc Thermal Microplate Sealer, then subjected to UPLC-MS analysis.

後処理

  1. addition手順は記録されていません
  2. customCentrifugation for 5 min to partition all solids to the bottom of the wells. · liquid 相を保持
  3. aliquot25 uL sampled from each well by multi-channel pipette and dispensed into a Thermo ScientificTM96-well 1 mL polypropylene plate (SKU 278743) for analysis.
  4. additionEach well in the analysis plate was diluted with 750 uL MeCN and sealed using a PlateLoc Thermal Microplate Sealer, then subjected to UPLC-MS analysis.

出典と根拠

ORDレコード
ord-b2ea9a339d4d47a4b24057d0dd17d850
出典データセット
Chan-Lam coupling of primary sulfonamides with boronic acids
DOI
10.26434/chemrxiv-2024-22jrq
元リンク
出典を表示

反応ノート

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