Carbanilide → HCID 59334949, compound

HRID 1517933Notes

Reaction equation

HRID 1517933 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([S:9]([NH:12][C:13]2[CH:14]=[C:15]3[C:19](=[CH:20][CH:21]=2)[NH:18][CH:17]=[CH:16]3)(=[O:11])=[O:10])[CH:5]=[C:6]([Cl:8])[CH:7]=1.[CH:22]1[CH:23]=[CH:24][C:25]([NH:28][C:29](NC2C=CC=CC=2)=[O:30])=[CH:26][CH:27]=1>>[C:25]1([NH:28][C:29]([N:18]2[C:19]3[C:15](=[CH:14][C:13]([NH:12][S:9]([C:4]4[CH:3]=[C:2]([Cl:1])[CH:7]=[C:6]([Cl:8])[CH:5]=4)(=[O:11])=[O:10])=[CH:21][CH:20]=3)[CH:16]=[CH:17]2)=[O:30])[CH:26]=[CH:27][CH:22]=[CH:23][CH:24]=1

Participants

3

Reactant 2

HCID 7595CarbanilideHCID 25044530HCID 25044530, compound

Product 1

HCID 59334949HCID 59334949, compound

Procedure

Yield: 124 mg (the product also contains 3,5-dichloro-N-(1H-indol-5-yl)-phenylsulphonamide and diphenylurea)

Sources & evidence

ORD record
ord-1c0f3d5f98024039b4168c898fa8047a
Source dataset
uspto-grants-2012_07
Patent number
US08232312B2

Reaction notes

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