Sulfuryl chloride → 2-Chloro-3-(3-oxomorpholino)benzene-1-sulfonyl chloride
Reaction equation
C(S[C:9]1[C:10]([Cl:22])=[C:11]([N:15]2[CH2:20][CH2:19][O:18][CH2:17][C:16]2=[O:21])[CH:12]=[CH:13][CH:14]=1)C1C=CC=CC=1.[S:23]([Cl:27])(Cl)(=[O:25])=[O:24]>>[Cl:22][C:10]1[C:11]([N:15]2[CH2:20][CH2:19][O:18][CH2:17][C:16]2=[O:21])=[CH:12][CH:13]=[CH:14][C:9]=1[S:23]([Cl:27])(=[O:25])=[O:24]Participants
3
Procedure
Intermediate 10 (1 g, 3.05 mmol) was converted to the title sulfonyl chloride using the procedure described in example 1; 1.6). The crude material was used without further purification in the next step.
Workup
- customThe crude material was used without further purification in the next step
Sources & evidence
- ORD record
- ord-52c3bb1605b04288803e6791658d757d
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08835653B2
Reaction notes
Loading…