Sodium Hydroxide → 4-(4-amino-2-propyl-2H-pyrazolo[3,4-c]quinolin-1-yl)butan-1-ol

HRID 1360528노트

반응식

HRID 1360528 반응식
[OH:1][CH2:2][CH2:3][CH2:4][CH2:5][C:6]1[N:7]([CH2:34][CH2:35][CH3:36])[N:8]=[C:9]2[C:18]=1[C:17]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[N:11]=[C:10]2[N:19](C(OC(C)(C)C)=O)C(OC(C)(C)C)=O.[OH-].[Na+]>Cl.C(O)C.CO>[NH2:19][C:10]1[C:9]2=[N:8][N:7]([CH2:34][CH2:35][CH3:36])[C:6]([CH2:5][CH2:4][CH2:3][CH2:2][OH:1])=[C:18]2[C:17]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[N:11]=1

참가 물질

6

실험 절차

A solution of di(tert-butyl) 1-(4-hydroxybutyl)-2-propyl-2H-pyrazolo[3,4-c]quinolin-4-ylimidodicarbonate (prepared as described in Parts A-C of Example 57, 0.507 g, 1.02 mmol) in 6 M HCl in ethanol (5 mL) was heated at 60° C. for 1.5 hours. The solution was allowed to cool to room temperature, and then was concentrated under reduced pressure to yield an oil. The oil was triturated with ether to obtain a solid that was isolated by filtration. The solid was dissolved in methanol and the solution was adjusted to approximately pH 14 with 50% aqueous sodium hydroxide. The solution was concentrated under reduced pressure and the crude product was purified by chromatography (silica gel, elution with 5% CMA in chloroform) followed by crystallization from hexanes/ethyl acetate to provide 0.084 g of 4-(4-amino-2-propyl-2H-pyrazolo[3,4-c]quinolin-1-yl)butan-1-ol as white needles, mp 135.0-136.0° C.

후처리

  1. concentrationwas concentrated under reduced pressure
  2. customto yield an oil
  3. customThe oil was triturated with ether
  4. customto obtain a solid
  5. customthat was isolated by filtration
  6. concentrationThe solution was concentrated under reduced pressure
  7. customthe crude product was purified by chromatography (silica gel, elution with 5% CMA in chloroform)
  8. customfollowed by crystallization from hexanes/ethyl acetate

출처 및 근거

ORD 기록
ord-b857e44fcdb6417ea13ab5e7253213a5
출처 데이터셋
uspto-grants-2011_02
특허 번호
US07879849B2

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