Trimethyl borate → 3-(3-Heptyl-1-methylureido)phenylboronic acid

HRID 250930

反応式

HRID 250930 の反応式
Br[C:2]1[CH:3]=[C:4]([N:8]([CH3:19])[C:9]([NH:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])=[O:10])[CH:5]=[CH:6][CH:7]=1.C[Li].C([Li])(C)(C)C.[B:27](OC)([O:30]C)[O:28]C>O1CCCC1.CCCCC>[CH2:12]([NH:11][C:9](=[O:10])[N:8]([C:4]1[CH:3]=[C:2]([B:27]([OH:30])[OH:28])[CH:7]=[CH:6][CH:5]=1)[CH3:19])[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]

参加物

7

反応物 4

HCID 8470Trimethyl borateHCID 116168371-(3-Bromophenyl)-3-heptyl-1-methylureaHCID 178418306HCID 178418306、化合物HCID 178418348HCID 178418348、化合物

生成物 1

HCID 115583693-(3-Heptyl-1-methylureido)phenylboronic acid収率 36%

試薬・触媒・溶媒 2

HCID 8003Pentane溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

In a manner similar to that of Example (18a), by reaction of 113 g (0.345 mol, 1 eq) of 1-(3-bromophenyl)-3-heptyl-1-methylurea in 1.13 L of tetrahydrofuran, 127 mL (0.38 mol, 1.1 eq) of methyllithium, 530 mL (0.76 mol, 2.2 eq) of a 1.7M solution of tert-butyllithium in pentane and 97 mL (0.904 mol, 2.2 eq) of trimethyl borate, and after purification by chromatography on silica gel (50/50 heptane/ethyl acetate) and crystallization from ethyl acetate/heptane, 36.0 g of 3-(3-heptyl-1-methylureido)phenylboronic acid are obtained in the form of a pinkish powder. Yield=36%

後処理

  1. customafter purification by chromatography
  2. customon silica gel (50/50 heptane/ethyl acetate) and crystallization from ethyl acetate/heptane, 36.0 g of 3-(3-heptyl-1-methylureido)phenylboronic acid
  3. customare obtained in the form of a pinkish powder

出典と根拠

ORDレコード
ord-a4d70830b5e943f6adba87c891408446
出典データセット
uspto-grants-2011_01
特許番号
US07863332B2

関連ノート

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