HCID 6465104, compound → HCID 68680371, compound

HRID 2265898Notes

Reaction equation

HRID 2265898 reaction equation
C[O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH2:10][NH:11][S:12]([C:15]1[CH:20]=[CH:19][C:18]([CH3:21])=[CH:17][CH:16]=1)(=[O:14])=[O:13].FC1C=CC(OC2C=CC(S(NCCC3C=CC=CC=3O)(=O)=O)=CC=2)=CC=1>>[OH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH2:10][NH:11][S:12]([C:15]1[CH:16]=[CH:17][C:18]([CH3:21])=[CH:19][CH:20]=1)(=[O:14])=[O:13]

Participants

3

Reactant 2

HCID 6465104HCID 6465104, compoundHCID 66879234HCID 66879234, compound

Product 1

HCID 68680371HCID 68680371, compound

Procedure

The title compound is prepared starting from N-[2-(2-methoxyphenyl)ethyl]-4-methylbenzenesulfonamide in analogy to the method described under 19B, it likewise being possible for the crude product to be reacted further without further purification.

Workup

  1. customto be reacted further without further purification

Sources & evidence

ORD record
ord-6def471736164d988dd9ede3fd8e3eb6
Source dataset
uspto-grants-2010_12
Patent number
US07858619B2

Reaction notes

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