5-Nitroindazole → HCID 22315789, compound

HRID 1707225Notes

Reaction equation

HRID 1707225 reaction equation
[NH+]1NN=NC=1.C(C1C=CC(S([O-])(=O)=O)=CC=1)CCCCCCCCCCC.[Na+].[N+:29]([C:32]1[CH:33]=[C:34]2[C:38](=[CH:39][CH:40]=1)[NH:37][N:36]=[CH:35]2)([O-])=[O:30]>>[N:29]([C:32]1[CH:33]=[C:34]2[C:38](=[CH:39][CH:40]=1)[NH:37][N:36]=[CH:35]2)=[O:30]

Participants

4

Reactant 3

HCID 215015-NitroindazoleHCID 4289524Sodium 4-dodecylbenzenesulfonateHCID 24785025HCID 24785025, compound

Product 1

HCID 22315789HCID 22315789, compound

Procedure

Next, a protective layer to which were added 700 ml/mol Ag of tetrazolium compound T-6 represented by Formula T, 300 mg of sodium p-dodecylbenzenesulfonate and 80 mg/mol Ag of 5-nitroindazole was coated according to double-jet process, and this was designated as Sample (1). Also, a protective layer, to which 5-nitrosoindazole and 2.5 g per mol of Ag of cyclodextrin Isoelite P, produced by Ensuikoseito Co., were added, was coated also according to double-jet process. This was designated as Sample (2).

Sources & evidence

ORD record
ord-44a1f8e3aa3e44b69b8c9878b6aed371
Source dataset
uspto-grants-1994_10
Patent number
US05352563

Reaction notes

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