Chlorosulfamic acid → HCID 66747228, compound
Reaction equation
[NH2:1][C:2]1[C:3]([C:19]#[N:20])=[C:4]([CH:16]=[CH:17][CH:18]=1)[O:5][CH2:6][C:7]([NH:10][C:11](=[O:15])[CH2:12][CH2:13][CH3:14])([CH3:9])[CH3:8].[S:21](Cl)(=[O:24])(=[O:23])[NH2:22]>>[S:21]([NH:1][C:2]1[C:3]([C:19]#[N:20])=[C:4]([CH:16]=[CH:17][CH:18]=1)[O:5][CH2:6][C:7]([NH:10][C:11](=[O:15])[CH2:12][CH2:13][CH3:14])([CH3:9])[CH3:8])(=[O:24])(=[O:23])[NH2:22]Participants
3
Procedure
Prepared as in Example 215a from N-(1-(3-amino-2-cyanophenoxy)-2-methylpropan-2-yl)butyramide (Example 229b) and sulfamoyl chloride in 100% yield. MS 355 (MH+).
Sources & evidence
- ORD record
- ord-f8852fac17dd4a33ae30a02dc680d45a
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09181276B2
Reaction notes
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