Methyl 4-chloroacetoacetate → HCID 22638652, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([NH2:9])=[S:8])=[CH:5][N:4]=1.Cl[CH2:13][C:14](=O)[CH2:15][C:16]([O:18][CH3:19])=[O:17]>>[CH3:1][O:2][C:3]1[N:4]=[CH:5][C:6]([C:7]2[S:8][CH:13]=[C:14]([CH2:15][C:16]([O:18][CH3:19])=[O:17])[N:9]=2)=[CH:10][CH:11]=1Participants
3
Procedure
This material was prepared according to the procedure described for Example 24(a) using 6-methoxythionicotinamide (Maybridge) (1.68 g, 10.0 mmol) and methyl 4-chloroacetoacetate (1.42 g, 10.0 mmol). Chromatography (gradient elution: 0-20% EtOAc in hexanes) of the crude material afforded the compound as an off-white solid. MS m/z: 265 (M+1). Calc'd for C12H12N2O3S: 264.06.
Workup
- customThis material was prepared
- washChromatography (gradient elution: 0-20% EtOAc in hexanes) of the crude material
Sources & evidence
- ORD record
- ord-75531a77d02a4ebdab18add0464786c0
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06822097B1
Reaction notes
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