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

HRID 266916
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HRID 266916 반응식
[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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
25 °C

실험 절차

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.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  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

출처 및 근거

ORD 기록
ord-a0108b003d4f4800933b37f2cf7a7115
출처 데이터셋
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05652363

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