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Potassium Carbonate → HCID 23653815、化合物

HRID 597923
ノート
印刷プレビュー

反応式

HRID 597923 の反応式
BrC1C(OC)=NC2CCN(C(=O)C(F)(F)F)CC(C)C=2C=1.[Sn](C=C)(CCCC)(CCCC)CCCC.[CH3:37][O:38][C:39]1[C:40]([CH:57]=[CH2:58])=[CH:41][C:42]2[CH:48]([CH3:49])[CH2:47][N:46](C(=O)C(F)(F)F)[CH2:45][CH2:44][C:43]=2[N:56]=1.C([O-])([O-])=O.[K+].[K+]>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.O.CO.C1(C)C=CC=CC=1>[CH3:37][O:38][C:39]1[C:40]([CH:57]=[CH2:58])=[CH:41][C:42]2[CH:48]([CH3:49])[CH2:47][NH:46][CH2:45][CH2:44][C:43]=2[N:56]=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

9

反応物 4

HCID 11430Potassium CarbonateHCID 81998TributylvinyltinHCID 23654109HCID 23654109、化合物HCID 23654281HCID 23654281、化合物

生成物 1

HCID 23653815HCID 23653815、化合物収率 77%

試薬・触媒・溶媒 4

HCID 178418397
HCID 178418397、化合物
触媒
HCID 887Methanol溶媒
HCID 962Water溶媒
HCID 1140Toluene溶媒

反応条件

温度
110 °C

実験手順

A mixture of 3-bromo-2-methoxy-5-methyl-7-(trifluoroacetyl)-6,7,8,9-tetrahydro -5H-pyrido[2,3-d]azepine (220 mg, 599 μmol), Bu3SnCH═CH2 (523 μl, 1.79 mmol), Pd(PPh3)4 (50 mg), and toluene (10 ml) was heated in a sealed tube at 110° C. for 16 h. The solvent was evaporated and the resulting residue was purified by column chromatography to render 165 mg (88%) of 2-methoxy-5-methyl-7-(trifluoroacetyl)-3-vinyl-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine. A mixture of 2-methoxy-5-methyl-7-(trifluoroacetyl)-3-vinyl-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine (32 mg, 102 μmol), K2CO3 (40 mg), MeOH (5 ml) and H2O (1 ml) was heated to reflux for 10 min. The reaction mixture was concentrated in vacuo and the resulting residue was purified by column chromatography to yield 17.0 mg (77%) of 2-methoxy-5-methyl-3-vinyl-6,7,8,9-tetrahydro-5H-pyrido[2,3-d]azepine. 1H-NMR (CDCl3) δ 7.58 (s, 1H), 6.92 (dd, 1H), 5.86 (d, 1H), 5.40 (d, 1H), 4.02 (s, 3H), 3.60-3.40 (m, 4H), 3.31 (m, 1H), 3.18 (dd, 1H), 3.00 (m, 1H), 1.52 (d, 3H) ppm.

後処理

  1. customThe solvent was evaporated
  2. customthe resulting residue was purified by column chromatography
  3. temperaturewas heated
  4. temperatureto reflux for 10 min
  5. concentrationThe reaction mixture was concentrated in vacuo
  6. customthe resulting residue was purified by column chromatography

出典と根拠

ORDレコード
ord-2c04d402e6e44850ac4d80f992ca9724
出典データセット
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07897595B2

反応ノート

読み込み中…

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