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Trimethyl borate → 3-(1-Methyl-3-pentylureido)phenylboronic acid

HRID 250909
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HRID 250909 반응식
Br[C:2]1[CH:3]=[C:4]([N:8]([CH3:17])[C:9]([NH:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])=[O:10])[CH:5]=[CH:6][CH:7]=1.C[Li].C([Li])(C)(C)C.[B:25](OC)([O:28]C)[O:26]C>O1CCCC1.CCCCC>[CH3:17][N:8]([C:4]1[CH:3]=[C:2]([B:25]([OH:28])[OH:26])[CH:7]=[CH:6][CH:5]=1)[C:9]([NH:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 8470Trimethyl borateHCID 672727941-(3-Bromophenyl)-1-methyl-3-pentylureaHCID 178418306HCID 178418306, 화합물HCID 178418348HCID 178418348, 화합물

생성물 1

HCID 672732723-(1-Methyl-3-pentylureido)phenylboronic acid수율 39%

시약·촉매·용매 2

HCID 8003Pentane
용매
HCID 8028Tetrahydrofuran용매

실험 절차

In a manner similar to that of Example (18a), by reaction of 123 g (0.411 mol, 1 eq) of 1-(3-bromophenyl)-1-methyl-3-pentylurea in 1.23 L of tetrahydrofuran, 150 mL (0.452 mol, 1.1 eq) of methyllithium, 530 mL (0.904 mol, 2.2 eq) of a 1.7 M solution of tert-butyllithium in pentane and 115 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, 42.0 g of 3-(1-methyl-3-pentylureido)phenylboronic acid are obtained in the form of a pink-colored powder. Yield=39%

후처리

  1. customafter purification by chromatography
  2. customon silica gel (50/50 heptane/ethyl acetate) and crystallization from ethyl acetate/heptane, 42.0 g of 3-(1-methyl-3-pentylureido)phenylboronic acid
  3. customare obtained in the form of a pink-colored powder

출처 및 근거

ORD 기록
ord-b51e54c96bc14c959fc6dba60834ce53
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07863332B2

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