Chlorosulfamic acid → HCID 67399904, compound
Reaction equation
[C:1]([O:4][CH:5]([CH:20]([CH3:22])[CH3:21])[C:6]([CH3:19])([CH3:18])[CH2:7][O:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([NH2:15])[C:10]=1[C:16]#[N:17])(=[O:3])[CH3:2].[S:23](Cl)(=[O:26])(=[O:25])[NH2:24]>>[C:1]([O:4][CH:5]([CH:20]([CH3:22])[CH3:21])[C:6]([CH3:19])([CH3:18])[CH2:7][O:8][C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([NH:15][S:23](=[O:26])(=[O:25])[NH2:24])[C:10]=1[C:16]#[N:17])(=[O:3])[CH3:2]Participants
3
Procedure
Prepared as in Example 215a from 1-(3-amino-2-cyanophenoxy)-2,2,4-trimethylpentan-3-yl acetate (Example 243b) and sulfamoyl chloride in 90% yield. MS 384 (MH+).
Sources & evidence
- ORD record
- ord-3e60b7b775a54a6fbc634269ab212f04
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09181276B2
Reaction notes
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