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HCID 18449249, 화합물 → HCID 18449206, 화합물

HRID 1270173
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HRID 1270173 반응식
[CH:1]([NH:4][C:5]1[C:6]2[N:7]([C:22]([O:25]C)=[N:23][N:24]=2)[C:8]2[C:13]([N:14]=1)=[CH:12][C:11]([CH2:15][N:16]1[CH2:21][CH2:20][O:19][CH2:18][CH2:17]1)=[CH:10][CH:9]=2)([CH3:3])[CH3:2]>CC(O)=O.Br>[CH:1]([NH:4][C:5]1[C:6]2[N:7]([C:22](=[O:25])[NH:23][N:24]=2)[C:8]2[C:13]([N:14]=1)=[CH:12][C:11]([CH2:15][N:16]1[CH2:17][CH2:18][O:19][CH2:20][CH2:21]1)=[CH:10][CH:9]=2)([CH3:3])[CH3:2]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 18449249HCID 18449249, 화합물

생성물 1

HCID 18449206HCID 18449206, 화합물

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 260Hydrogen Bromide용매

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온도
23 °C

실험 절차

A solution of isopropyl-(1-methoxy-7-morpholin-4-ylmethyl-[1,2,4]triazolo[4,3-a]quinoxalin-4-yl)-amine (32 mg) in AcOH (0.5 mL) and 48% HBr (0.5 mL) was heated at 50° C. for 2.5 hrs. After cooling to 23° C., the solution was concentrated. The resulting residue was concentrated from toluene, and then triturated with MeOH/EtOAc. The resulting solid was isolated by filtration, and then concentrated from MeOH to afford a light yellow solid. MS (M+H)+=341.3.

후처리

  1. concentrationthe solution was concentrated
  2. concentrationThe resulting residue was concentrated from toluene
  3. customtriturated with MeOH/EtOAc
  4. customThe resulting solid was isolated by filtration
  5. concentrationconcentrated from MeOH
  6. customto afford a light yellow solid

출처 및 근거

ORD 기록
ord-5201cece30de47daa93faafd590f12d9
출처 데이터셋
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07202245B2

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