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 17 (1 g, 3.05 mmol) was converted to the title sulfonyl chloride using the procedure described in 1.7). 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-e50177b8f36747a3866f1aa156c749f9
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08378092B2
Reaction notes
Loading…