Water → 1-Cyclohexyloxycarbonyloxyethyl 3-(6-aminopyridin-3-yl)-2-(1-cyclohexyl-1H-imidazol-4-yl)propionate

HRID 2370916노트

반응식

HRID 2370916 반응식
Cl.[NH2:2][C:3]1[N:8]=[CH:7][C:6]([CH2:9][CH:10]([C:14]2[N:15]=[CH:16][N:17]([CH:19]3[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]3)[CH:18]=2)[C:11]([OH:13])=[O:12])=[CH:5][CH:4]=1.[CH:25]1([O:31][C:32]([O:34][CH:35](Cl)[CH3:36])=[O:33])[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26]1.C([O-])([O-])=O.[K+].[K+].O>CN(C=O)C>[NH2:2][C:3]1[N:8]=[CH:7][C:6]([CH2:9][CH:10]([C:14]2[N:15]=[CH:16][N:17]([CH:19]3[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]3)[CH:18]=2)[C:11]([O:13][CH:35]([O:34][C:32]([O:31][CH:25]2[CH2:30][CH2:29][CH2:28][CH2:27][CH2:26]2)=[O:33])[CH3:36])=[O:12])=[CH:5][CH:4]=1

참가 물질

6

실험 절차

A solution of 50.0 mg (0.16 mmol) of the compound from example 1i and 39 mg (0.19 mmol) of 1-cyclohexyloxycarbonyloxy-1-ethyl chloride, 13 mg (0.08 mmol) of KI and 26 mg (0.19 mmol) of K2CO3 in 2 ml of DMF was stirred at 60° C. for 12 h. Then 5 ml of water were added and the reaction solution was extracted several times with EA. The combined EA extracts were dried, filtered and concentrated to dryness. The resulting residue was purified on silica gel with CH2Cl2/methanol as mobile phase, resulting in 32 mg of the title compound in the form of an amorphous solid.

후처리

  1. extractionthe reaction solution was extracted several times with EA
  2. dry with materialThe combined EA extracts were dried
  3. filtrationfiltered
  4. concentrationconcentrated to dryness
  5. customThe resulting residue was purified on silica gel with CH2Cl2/methanol as mobile phase

출처 및 근거

ORD 기록
ord-cc0d635853b74da9a230ff0d40108b32
출처 데이터셋
uspto-grants-2014_04
특허 번호
US08710232B2

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