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4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline → 5-(5-amino-2-methylphenyl)-1-methyl-3-morpholinopyridin-2(1H)-one

HRID 594084
ノート
印刷プレビュー

反応式

HRID 594084 の反応式
Br[C:2]1[CH:3]=[C:4]([N:10]2[CH2:15][CH2:14][O:13][CH2:12][CH2:11]2)[C:5](=[O:9])[N:6]([CH3:8])[CH:7]=1.[CH3:16][C:17]1[CH:23]=[CH:22][C:20]([NH2:21])=[CH:19][C:18]=1B1OC(C)(C)C(C)(C)O1>COCCOC.C(=O)([O-])[O-].[Na+].[Na+].C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C(Cl)Cl>[NH2:21][C:20]1[CH:19]=[CH:18][C:17]([CH3:16])=[C:23]([C:2]2[CH:3]=[C:4]([N:10]3[CH2:15][CH2:14][O:13][CH2:12][CH2:11]3)[C:5](=[O:9])[N:6]([CH3:8])[CH:7]=2)[CH:22]=1
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

6

反応物 2

HCID 160860894-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 904089385-bromo-1-methyl-3-morpholinopyridin-2(1H)-one

生成物 1

HCID 904081725-(5-amino-2-methylphenyl)-1-methyl-3-morpholinopyridin-2(1H)-one収率 31%

試薬・触媒・溶媒 3

HCID 178418807HCID 178418807、化合物触媒HCID 8071
1,2-Dimethoxyethane
溶媒
HCID 10340Sodium Carbonate溶媒

反応条件

温度
120 °C

実験手順

To a solution of 5-bromo-1-methyl-3-morpholinopyridin-2(1H)-one (1.0 equiv.) and 4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (1.2 equiv.) in DME and 2M sodium carbonate (3:1, 0.14 M) was added PdCl2(dppf)-DCM adduct (0.1 equiv.) in a microwave vial equipped with a stir bar. The reaction was heated to 120° C. for 15 min in the microwave. The solution was partitioned between water and ethyl acetate, the organic phase was dried with sodium sulfate, filtered and concentrated. The crude material was purified via silica gel column chromatography eluting with 100% ethyl acetate followed by 10% methanol in ethyl acetate. The pure fractions were concentrated and dried under vacuo to afford 5-(5-amino-2-methylphenyl)-1-methyl-3-morpholinopyridin-2(1H)-one in 31% yield. LCMS (m/z) (M+H)=300.2, Rt=0.41 min.

後処理

  1. customvial equipped with a stir bar
  2. customThe solution was partitioned between water and ethyl acetate
  3. dry with materialthe organic phase was dried with sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude material was purified via silica gel column chromatography
  7. washeluting with 100% ethyl acetate
  8. concentrationThe pure fractions were concentrated
  9. customdried under vacuo

出典と根拠

ORDレコード
ord-a229ebc32e34438fbf9a1118d1bf94fb
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09242969B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート