Ethanol → HCID 58930873, compound
Reaction equation
[Cl-].[NH4+].C(O)C.O1CCCC1.[CH2:11]([O:18][C:19]1[CH:24]=[CH:23][C:22]([C:25]2[N:44]([CH2:45][O:46][CH2:47][CH2:48][Si:49]([CH3:52])([CH3:51])[CH3:50])[C:28]3[N:29]=[CH:30][N:31]=[C:32]([O:33][C:34]4[CH:39]=[CH:38][C:37]([N+:40]([O-])=O)=[C:36]([F:43])[CH:35]=4)[C:27]=3[CH:26]=2)=[CH:21][CH:20]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>[Fe].O>[CH2:11]([O:18][C:19]1[CH:24]=[CH:23][C:22]([C:25]2[N:44]([CH2:45][O:46][CH2:47][CH2:48][Si:49]([CH3:52])([CH3:51])[CH3:50])[C:28]3[N:29]=[CH:30][N:31]=[C:32]([O:33][C:34]4[CH:39]=[CH:38][C:37]([NH2:40])=[C:36]([F:43])[CH:35]=4)[C:27]=3[CH:26]=2)=[CH:21][CH:20]=1)[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 85 °C
Procedure
After adding 400 mg of iron powder, 1 g of ammonium chloride, 20 ml of ethanol, 10 ml of tetrahydrofuran and 10 ml of water to 470 mg of 6-(4-benzyloxyphenyl)-4-(3-fluoro-4-nitrophenoxy)-7-(trimethylsilanylethoxymethyl)-7H-pyrrolo[2,3-d]pyrimidine, the mixture was stirred at 85° C. for 3 hours. After returning it to room temperature, it was filtered with celite, and ethyl acetate and water were added to the filtrate for liquid separation and extraction. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, filtered with plug cotton, concentrated and subjected to NH silica gel column chromatography (hexane-ethyl acetate) to obtain 263 mg of the title compound.
Workup
- customto room temperature
- filtrationit was filtered with celite, and ethyl acetate and water
- additionwere added to the filtrate for liquid separation and extraction
- washThe organic layer was washed with saturated brine
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered with plug cotton
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-c19efa37cc5642d091a801c7c500e3b1
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07253286B2
Reaction notes
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