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Hydrochloric Acid → HCID 178442450, 화합물

HRID 216382
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인쇄 미리보기

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HRID 216382 반응식
Cl.[CH3:2][C:3]([CH3:47])([CH2:45][CH3:46])[CH2:4][C:5]1[N:6]=[C:7]([CH2:29][CH:30]([C:32]2[CH:37]=[CH:36][C:35]([C:38]3[CH:43]=[CH:42][C:41]([F:44])=[CH:40][N:39]=3)=[CH:34][CH:33]=2)[NH2:31])[N:8](C(C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[CH:9]=1>CO>[CH3:2][C:3]([CH3:47])([CH2:45][CH3:46])[CH2:4][C:5]1[N:6]=[C:7]([CH2:29][CH:30]([C:32]2[CH:37]=[CH:36][C:35]([C:38]3[CH:43]=[CH:42][C:41]([F:44])=[CH:40][N:39]=3)=[CH:34][CH:33]=2)[NH2:31])[NH:8][CH:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 686682132-[4-(2,2-dimethylbutyl)-1-trityl-1H-imidazol-2-yl]-1-[4-(5-fluoropyridin-2-yl)phenyl]ethanamine

생성물 1

HCID 178442450HCID 178442450, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
60 °C

실험 절차

Hydrogen chloride (4 M in dioxane) (2 mL, 0.5 mmol) was added to a solution of 2-[4-(2,2-dimethylbutyl)-1-trityl-1H-imidazol-2-yl]-1-[4-(5-fluoropyridin-2-yl)phenyl]ethanamine (20 mg, 0.03 mmol) in methanol (6 mL). After stirring at 60° C. for 1 h, volatiles were removed. The residue was purified by preparative HPLC eluting with 10-50% acetonitrile/water and lyophilized to afford the title compound. (M+H) found 367.

후처리

  1. customvolatiles were removed
  2. customThe residue was purified by preparative HPLC
  3. washeluting with 10-50% acetonitrile/water

출처 및 근거

ORD 기록
ord-efc5bd990e3949a3a8f8b440085f15c6
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08193228B2

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