4-t-Butylbenzenesulfonyl chloride → HCID 58978317, compound

HRID 2115380Notes

Reaction equation

HRID 2115380 reaction equation
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([NH:8][C:9](=[O:11])[CH3:10])=[N:6][CH:7]=1.[C:12]([C:16]1[CH:21]=[CH:20][C:19]([S:22](Cl)(=[O:24])=[O:23])=[CH:18][CH:17]=1)([CH3:15])([CH3:14])[CH3:13]>>[C:12]([C:16]1[CH:21]=[CH:20][C:19]([S:22]([NH:1][C:2]2[CH:3]=[CH:4][C:5]([NH:8][C:9](=[O:11])[CH3:10])=[N:6][CH:7]=2)(=[O:24])=[O:23])=[CH:18][CH:17]=1)([CH3:15])([CH3:13])[CH3:14]

Participants

3

Reactant 2

HCID 1398824-t-Butylbenzenesulfonyl chlorideHCID 27352192-Acetamido-5-aminopyridine

Product 1

HCID 58978317HCID 58978317, compound

Procedure

prepared by reaction of N-(5-amino-pyridin-2-yl)-acetamide with 4-tert-butyl-benzene-sulfonyl chloride

Sources & evidence

ORD record
ord-0e7b450dba9f42f588075fdfbc98dcaa
Source dataset
uspto-grants-2008_10
Patent number
US07435815B2

Reaction notes

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