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Ammonia → 1-(2-aminoethyl)-1H-imidazo[4,5-c]quinoline-2,4-diamine

HRID 1097600
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HRID 1097600 반응식
[NH2:1][C:2]1[N:3]([CH2:16][CH2:17][NH:18]C(=O)OC(C)(C)C)[C:4]2[C:13]3[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=3[N:7]=[C:6](Cl)[C:5]=2[N:15]=1.[NH3:26]>CO>[NH2:18][CH2:17][CH2:16][N:3]1[C:4]2[C:13]3[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=3[N:7]=[C:6]([NH2:26])[C:5]=2[N:15]=[C:2]1[NH2:1]
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참가 물질

4

반응물 2

HCID 222AmmoniaHCID 86626304tert-butyl 2-(2-amino-4-chloro-1H-imidazo[4,5-c]quinolin-1-yl)ethylcarbamate

생성물 1

HCID 668145001-(2-aminoethyl)-1H-imidazo[4,5-c]quinoline-2,4-diamine

시약·촉매·용매 1

HCID 887Methanol용매

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온도
150 °C

실험 절차

tert-Butyl 2-(2-amino-4-chloro-1H-imidazo[4,5-c]quinolin-1-yl)ethylcarbamate (3.5 g, 9.7 mmol) and ammonia (approximately 100 mL of a 7 N solution in methanol) were added to a pressure vessel, which was sealed and heated at 150° C. overnight. The volatiles were removed under reduced pressure, and the residue was purified by automated flash chromatography (silica cartridge, eluting with aqueous ammonium hydroxide:methanol:dichloromethane in a gradient from 0:0:100 to 1.5:28.5:70) to provide 840 mg of 1-(2-aminoethyl)-1H-imidazo[4,5-c]quinoline-2,4-diamine as a dark grey solid.

후처리

  1. customwhich was sealed
  2. customThe volatiles were removed under reduced pressure
  3. customthe residue was purified by automated flash chromatography (silica cartridge
  4. washeluting with aqueous ammonium hydroxide

출처 및 근거

ORD 기록
ord-bd7fc6e343e044c1b5e4e539a9456fb4
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08143270B2

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