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Diisopropylethylamine → 4-bromo-2-fluoro-N-(pyrimidin-2-ylmethyl)benzamide

HRID 595810
ノート
印刷プレビュー

反応式

HRID 595810 の反応式
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=O)=[C:4]([F:11])[CH:3]=1.[N:12]1[CH:17]=[CH:16][CH:15]=[N:14][C:13]=1[CH2:18][NH2:19].CCN(C(C)C)C(C)C.C1CN([P+](ON2N=NC3C=CC=CC2=3)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F>CN(C=O)C>[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([NH:19][CH2:18][C:13]2[N:14]=[CH:15][CH:16]=[CH:17][N:12]=2)=[O:8])=[C:4]([F:11])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 81531DiisopropylethylamineHCID 3026814-Bromo-2-fluorobenzoic acidHCID 2724699PyBOPHCID 46580472-Pyrimidinemethanamine

生成物 1

HCID 1180457014-bromo-2-fluoro-N-(pyrimidin-2-ylmethyl)benzamide収率 29.3%

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

実験手順

To a flask was charged with 4-bromo-2-fluorobenzoic acid (180 mg, 0.821 mmol), pyrimidin-2-ylmethanamine (89.6 mg, 0.821 mmol), DIEA (0.358 mL, 2.05 mmol) in DMF (3 mL), and to the resulting solution was added PyBOP (513 mg, 0.915 mmol) and the resulting mixture was stirred at room temperature overnight, then was concentrated under reduced pressure and the residue was diluted with EtOAc (20 mL), washed with water (3×10 mL), brine (10 mL) and dried (Na2SO4), concentrated and the residue was purified by flash chromatography on silica gel eluted with gradient EtOAc/heptane (0-100%) and 4-bromo-2-fluoro-N-(pyrimidin-2-ylmethyl)benzamide (74.5 mg, 29.3%) was obtained as light color solid. LCMS (m/z): 310.0/312.0 (MH+), 0.64 min.

後処理

  1. concentrationwas concentrated under reduced pressure
  2. additionthe residue was diluted with EtOAc (20 mL)
  3. washwashed with water (3×10 mL), brine (10 mL)
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated
  6. customthe residue was purified by flash chromatography on silica gel
  7. washeluted with gradient EtOAc/heptane (0-100%)

出典と根拠

ORDレコード
ord-bbbb1bd250ff4f17b79b7994733f1a00
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09242996B2

反応ノート

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