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HCID 69057961, 화합물 → 5-amino-N-benzylnaphthalene-1-carboxamide

HRID 1818069
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HRID 1818069 반응식
[CH2:1]([NH:8][C:9]([C:11]1[C:20]2[C:15](=[C:16]([N+:21]([O-])=O)[CH:17]=[CH:18][CH:19]=2)[CH:14]=[CH:13][CH:12]=1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>[Pd].CO>[NH2:21][C:16]1[CH:17]=[CH:18][CH:19]=[C:20]2[C:15]=1[CH:14]=[CH:13][CH:12]=[C:11]2[C:9]([NH:8][CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 69057961HCID 69057961, 화합물

생성물 1

HCID 102147315-amino-N-benzylnaphthalene-1-carboxamide수율 88.7%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

5% Palladium on carbon (14 mg) was added to a suspension of N-benzyl-5-nitronaphthalene-1-carboxamide (128.0 mg, 0.418 mmol) in methanol (2.5 ml). The mixture was stirred at room temperature for 2 hours, under hydrogen atmosphere. After the palladium on carbon was filtered off, the filtrate was concentrated. The residue was solidified by a mixture of isopropyl ether: ethyl acetate (1:1), and the resulting solid was washed with isopropyl ether and dried to give the title compound as a light yellow solid (102 mg, 88.7%).

후처리

  1. filtrationAfter the palladium on carbon was filtered off
  2. concentrationthe filtrate was concentrated
  3. additionThe residue was solidified by a mixture of isopropyl ether: ethyl acetate (1:1)
  4. washthe resulting solid was washed with isopropyl ether
  5. customdried

출처 및 근거

ORD 기록
ord-25a9f81951214d0b860770bfa0811780
출처 데이터셋
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07598418B2

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