1-Chloroethyl chloroformate → HCID 22028200, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([S:8]([C:11]2[C:19]3[C:14](=[N:15][CH:16]=[CH:17][CH:18]=3)[N:13]([CH2:20][CH2:21][N:22](C)[CH3:23])[CH:12]=2)(=[O:10])=[O:9])[CH:5]=[CH:6][CH:7]=1.ClC(OC(Cl)C)=O>ClCCCl>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([S:8]([C:11]2[C:19]3[C:14](=[N:15][CH:16]=[CH:17][CH:18]=3)[N:13]([CH2:20][CH2:21][NH:22][CH3:23])[CH:12]=2)(=[O:10])=[O:9])[CH:5]=[CH:6][CH:7]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A stirred solution under nitrogen of N-(2-{3-[(3-chlorophenyl)sulfonyl]-1H-pyrrolo[2,3-b]pyridin-1-yl}ethyl)-N,N-dimethylamine (0.540 g, 1.49 mmol) in 1,2-dichloroethane is treated with 1-chloroethyl chloroformate (0.40 mL, 3.7 mmol), heated at reflux temperature for 2 h cooled, and concentrated in vacuo. The resultant residue is treated with ethanol, heated at reflux temperature for 2 h and concentrated in vacuo. This resultant residue is chromatographed using 2:98 concentrated NH4OH:ethanol as eluent to afford the free amine of the title product as a semi-solid (311 mg, 60%). The free amine is dissolved in ethanol, treated with 4M HCl in dioxane and filtered. The filtercake is dried to give the title product as a pale yellow solid, 274 mg (48% yield), mp 263-265° C. (dec.), identified by mass spectral and HNMR analyses.
Workup
- temperatureheated
- temperatureat reflux temperature for 2 h
- temperaturecooled
- concentrationconcentrated in vacuo
- additionThe resultant residue is treated with ethanol
- temperatureheated
- temperatureat reflux temperature for 2 h
- concentrationconcentrated in vacuo
- customThis resultant residue is chromatographed
Sources & evidence
- ORD record
- ord-58593f260ca44e5d936963fd71f5ef5e
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06825212B2
Reaction notes
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