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Dichloromethane → 2-Morpholin-4-yl-indan-5-ylamine

HRID 418361
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HRID 418361 반응식
[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[CH2:9][CH:8]([N:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1)[CH2:7]2)([O-])=O.C(Cl)Cl>CO.[Pd]>[N:13]1([CH:8]2[CH2:7][C:6]3[C:10](=[CH:11][CH:12]=[C:4]([NH2:1])[CH:5]=3)[CH2:9]2)[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6344DichloromethaneHCID 591907584-(5-Nitro-indan-2-yl)-morpholine

생성물 1

HCID 591908752-Morpholin-4-yl-indan-5-ylamine수율 101.3%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of 4-(5-nitro-indan-2-yl)-morpholine (210 mg, 0.85 mmol) in 20 mL of methanol was added Pd/C 10% (20 mg). The mixture was placed under a H2 atmosphere with stirring for 2 h. TLC showed 2 spots. CH2Cl2 was added to dissolve the ppt. that had formed and the hydrogenation continued further 2 h. The catalyst was removed by filtering, and the filtrate evaporated to give 188 mg of 2-morpholin-4-yl-indan-5-ylamine. The crude amine was used in the next step without purification.

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후처리

  1. dissolutionto dissolve the ppt
  2. customthat had formed
  3. waitthe hydrogenation continued further 2 h
  4. customThe catalyst was removed
  5. filtrationby filtering
  6. customthe filtrate evaporated

출처 및 근거

ORD 기록
ord-d4727b3e0ae345afb637f6fe94745554
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08093266B2

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