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Ammonium formate → 5-Amino-2-ethyl-2,3-dihydro-1H-isoindol-1-one

HRID 1947630
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HRID 1947630 반응식
[CH2:1]([N:3]1[CH2:11][C:10]2[C:5](=[CH:6][CH:7]=[C:8]([N+:12]([O-])=O)[CH:9]=2)[C:4]1=[O:15])[CH3:2].C([O-])=O.[NH4+]>CN(C=O)C.[Pd]>[NH2:12][C:8]1[CH:9]=[C:10]2[C:5](=[CH:6][CH:7]=1)[C:4](=[O:15])[N:3]([CH2:1][CH3:2])[CH2:11]2
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참가 물질

5

반응물 2

HCID 2723923Ammonium formateHCID 67223854HCID 67223854, 화합물

생성물 1

HCID 529112495-Amino-2-ethyl-2,3-dihydro-1H-isoindol-1-one수율 98.3%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 6228Dimethylformamide용매

실험 절차

Palladium/Carbon (10% wt) (63 mg, 0.30 mmol) was added to a stirred solution of 2-ethyl-5-nitro-2,3-dihydro-isoindol-1-one (634 mg, 3.06 mmol) and ammonium formate (949 mg, 15.31 mmol) in anhydrous DMF (12 ml) at room temperature. The resulting suspension was heated at reflux for 1 hr, then cooled and filtered through a pad of celite. The solvent was evaporated in vacuo and the crude residue purified by flash column chromatography (5% methanol in dichloromethane) to yield the title compound as a pale yellow oil (530 mg, 98%). HPLC retention time 0.95 min. Mass spectrum (ES+) m/z 177 (M+H).

후처리

  1. temperatureThe resulting suspension was heated
  2. temperatureat reflux for 1 hr
  3. temperaturecooled
  4. filtrationfiltered through a pad of celite
  5. customThe solvent was evaporated in vacuo
  6. customthe crude residue purified by flash column chromatography (5% methanol in dichloromethane)

출처 및 근거

ORD 기록
ord-299f0048b81743eda39b124a3739a2e3
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399481B2

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