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[3-(Adamantan-1-yl)-4-(benzyloxy)phenyl]boronic acid → ethyl(E)-3-{2-[3-(1-adamantyl)-4-benzyloxyphenyl]-5-pyrazinyl}-2-propenoate

HRID 508662
ノート
印刷プレビュー

反応式

HRID 508662 の反応式
[C:1]12([C:11]3[CH:12]=[C:13](B(O)O)[CH:14]=[CH:15][C:16]=3[O:17][CH2:18][C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.Br[C:29]1[N:30]=[CH:31][C:32](/[CH:35]=[CH:36]/[C:37]([O:39][CH2:40][CH3:41])=[O:38])=[N:33][CH:34]=1>COCCOC.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>[C:1]12([C:11]3[CH:12]=[C:13]([C:29]4[CH:34]=[N:33][C:32](/[CH:35]=[CH:36]/[C:37]([O:39][CH2:40][CH3:41])=[O:38])=[CH:31][N:30]=4)[CH:14]=[CH:15][C:16]=3[O:17][CH2:18][C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2
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

5

反応物 2

HCID 12134904[3-(Adamantan-1-yl)-4-(benzyloxy)phenyl]boronic acidHCID 53259408(E)-ethyl 3-(5-bromopyrazin-2-yl)acrylate

生成物 1

HCID 53259588ethyl(E)-3-{2-[3-(1-adamantyl)-4-benzyloxyphenyl]-5-pyrazinyl}-2-propenoate収率 91.4%

試薬・触媒・溶媒 2

HCID 178418397HCID 178418397、化合物触媒
HCID 8071
1,2-Dimethoxyethane
溶媒

反応条件

温度
90 °C

実験手順

To a solution of 3-(1-adamantyl)-4-benzyloxyphenylboronic acid (474 mg, 1.31 mmol) and ethyl(E)-3-(5-bromo-2-pyrazinyl)-2-propenoate (278 mg, 1.08 mmol) in DME (11 mL, degassed) was added tetrakis(triphenylphosphine)palladium (151 mg, 0.13 mmol) and degassed 2 M Na2CO3 (2.3 mL). The reaction mixture was heated at reflux (90° C. oil-bath) for 19.5 h, cooled to room temperature, and then diluted with EtOAc (155 mL). The organic layer was washed (H2O and brine) and dried. After solvent removal at reduced pressure, the residue was purified on silica gel (10% to 25% EtOAc/hexane) to give 488 mg (91%) of ethyl(E)-3-{2-[3-(1-adamantyl)-4-benzyloxyphenyl]-5-pyrazinyl}-2-propenoate as a yellow solid, mp 145-148° C. IR 2899, 1710, 1238 cm−1; 1H NMR δ (CDCl3) 1.35 (t, J=7.3 Hz, 3H, OCH2CH3), 1.73 (bs, 6H, AdCH2), 2.06 (bs, 3H, AdCH), 2.20 (bs, 6H, AdCH2), 4.29 (q, J=7.3 Hz, 2H, OCH2CH3), 5.19 (s, 2H, CH2), 6.98 (d, J=15.9 Hz, 1H, CH═CHCO), 7.04 (d, J=8.5 Hz, 1H, 5-ArH), 7.28-7.52 (m, 5H, C6H5), 7.72 (d, J=15.9 Hz, 1H, CH═CHCO), 7.84 (dd, J=8.5 Hz, 2.4 Hz, 1H, 6-ArH), 8.02 (d, J=2.4 Hz, 1H, 2-ArH), 8.63 (d, J=1.24 Hz, 1H, 3-PyrH), 8.99 ppm (d, J=1.24 Hz, 1H, 6-PyrH). HRMS calcd C32H34N2O3 [M+H]+ 495.2642. found 495.2659.

後処理

  1. customdegassed 2 M Na2CO3 (2.3 mL)
  2. temperatureThe reaction mixture was heated
  3. temperaturecooled to room temperature
  4. additiondiluted with EtOAc (155 mL)
  5. washThe organic layer was washed (H2O and brine)
  6. customdried
  7. customAfter solvent removal at reduced pressure
  8. customthe residue was purified on silica gel (10% to 25% EtOAc/hexane)

出典と根拠

ORDレコード
ord-38a9f136b4fe4fb693ed94e5753596ef
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09096544B2

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