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HCID 57799841, 화합물 → HCID 136055517, 화합물

HRID 2101086
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HRID 2101086 반응식
C([O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][C:18]=1[O:19][CH3:20])[C:15]([O:21][CH:22]([CH3:24])[CH3:23])=[N:14][C:13]([NH:25][C:26]1[CH:30]=[C:29]([CH3:31])[NH:28][N:27]=1)=[CH:12]2)C1C=CC=CC=1.[H][H]>[Pd].CO>[CH:22]([O:21][C:15]1[C:16]2[C:11](=[CH:10][C:9]([OH:8])=[C:18]([O:19][CH3:20])[CH:17]=2)[CH:12]=[C:13]([NH:25][C:26]2[CH:30]=[C:29]([CH3:31])[NH:28][N:27]=2)[N:14]=1)([CH3:24])[CH3:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 57799841HCID 57799841, 화합물HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 136055517HCID 136055517, 화합물수율 106.2%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A mixture of (6-benzyloxy-1-isopropoxy-7-methoxy-isoquinolin-3-yl)-(5-methyl-1H-pyrazol-3-yl)-amine (300 mg), 10% Pd/C (50 mg) and MeOH (80 ml) was shaken in Parr apparatus for 5 hs under 30-40 psi of hydrogen at room temperature. Then the mixture was passed through a celite pad and the filtrate was concentrated and dried to give 1-Isopropoxy-7-methoxy-3-(5-methyl-1H-pyrazol-3-ylamino)-isoquinolin-6-ol (250 mg). LC-MS: m/e 329 (MH+).

후처리

  1. concentrationthe filtrate was concentrated
  2. customdried

출처 및 근거

ORD 기록
ord-314ce3f93c68493dae8ef0df559c4728
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07572809B2

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