Methyl Acrylate → (E)-Methyl 3-(3-aminopyridin-2-YL)acrylate
反応式
[NH2:1][C:2]1[C:3](Br)=[N:4][CH:5]=[CH:6][CH:7]=1.[C:9]([O:13][CH3:14])(=[O:12])[CH:10]=[CH2:11].C(N(CC)CC)C>CC(P(C(C)(C)C)C1C=CC(N(C)C)=CC=1)(C)C.CC(P(C(C)(C)C)C1C=CC(N(C)C)=CC=1)(C)C.Cl[Pd]Cl.CN(C=O)C>[NH2:1][C:2]1[C:3](/[CH:11]=[CH:10]/[C:9]([O:13][CH3:14])=[O:12])=[N:4][CH:5]=[CH:6][CH:7]=1参加物
反応条件
- 温度
- 145 °C
実験手順
The following reaction was performed in duplicate: A glass microwave reaction vessel was charged with 3-amino-2-bromopyridine (2.00 g, 11.56 mmol) and bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) (0.250 g, 0.353 mmol). DMF (10 mL) was added followed by methyl acrylate (4.00 mL, 44.3 mmol) and triethylamine (4.00 mL, 28.7 mmol). The reaction mixture was sealed under argon and heated in an Initiator microwave reactor (Personal Chemistry, Biotage AB, Inc., Upssala, Sweden) at 145° C. for 40 min. The reaction mixtures were combined and the solvent was removed in vacuo. The residue was dissolved in DCM, evaporated onto silica gel and purified by flash chromatography (ISCO, (120 gram HP)) eluting with 2M NH3 in MeOH:CH2Cl2 (0:1-1:39) to give 2.75 g (69%) of a yellow amorphous solid. ESI-MS 179.0 [M+1].
後処理
- customThe following reaction
- customA glass microwave reaction vessel
- customThe reaction mixture was sealed under argon
- customThe reaction mixtures
- customthe solvent was removed in vacuo
- dissolutionThe residue was dissolved in DCM
- customevaporated onto silica gel
- custompurified by flash chromatography (ISCO, (120 gram HP))
- washeluting with 2M NH3 in MeOH:CH2Cl2 (0:1-1:39)
出典と根拠
- ORDレコード
- ord-a0156781118f47a7a0383180547625da
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09174992B2
反応ノート
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