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(Dimethyl sulfide)trihydroboron → 2,3-Dihydro-1H-pyrido[3,4-b][1,4]oxazine

HRID 266916
ノート
印刷プレビュー

反応式

HRID 266916 の反応式
[NH:1]1[C:6](=O)[CH2:5][O:4][C:3]2[CH:8]=[N:9][CH:10]=[CH:11][C:2]1=2.B.CSC>O1CCCC1>[NH:1]1[CH2:6][CH2:5][O:4][C:3]2[CH:8]=[N:9][CH:10]=[CH:11][C:2]1=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

4

反応物 2

HCID 12423031(Dimethyl sulfide)trihydroboronHCID 190316591H-Pyrido[3,4-b][1,4]oxazin-2(3H)-one

生成物 1

HCID 219615362,3-Dihydro-1H-pyrido[3,4-b][1,4]oxazine収率 70%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
25 °C

実験手順

To a stirred solution of 1H-pyrido-[3,4-b][1,4]oxazine-2-(3H)one (3 g, 21 mmol) in tetrahydrofuran (150 ml) was added rapidly a borane/dimethyl sulfide solution (52 ml of a 2M solution in THF, 5 eq) at 25° C. over 15 minutes. The reaction mixture was stirred at 25° C. for 2 hours and quenched with 5 ml of water. The solvent was removed in vacuo using a rotary evaporator and the residue treated with aqueous 1M HCl with stirring. The water was removed and the residue chromatographed on silica gel using CH2Cl2 /MeOH/NH4OH (90/10/1) to give 2 g (70%) of titled product. m.p. 167°-169° C. The structural assignment is supported by the proton NMR spectrum.

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

後処理

  1. customquenched with 5 ml of water
  2. customThe solvent was removed in vacuo
  3. customa rotary evaporator
  4. additionthe residue treated with aqueous 1M HCl
  5. stirringwith stirring
  6. customThe water was removed
  7. customthe residue chromatographed on silica gel

出典と根拠

ORDレコード
ord-a0108b003d4f4800933b37f2cf7a7115
出典データセット
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05652363

反応ノート

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