5-Aminosalicylic Acid → HCID 16051978, compound

HRID 2202207

Reaction equation

HRID 2202207 reaction equation
C1C=CN=C(NS(C2C=CC(N=N[C:19]3[CH:20]=[CH:21][C:22]([OH:28])=[C:23]([C:25]([OH:27])=[O:26])[CH:24]=3)=CC=2)(=O)=O)C=1.C1C([NH2:35])=CC(C(O)=O)=C(O)C=1.C1C(N=NC2C=CC(O)=C(C(O)=O)C=2)=CC(C(O)=O)=C(O)C=1.C1C(C(NCCC(O)=O)=O)=CC=C(N=NC2C=CC(O)=C(C(O)=O)C=2)C=1>>[NH2:35][O:28][C:22]1[C:23](=[CH:24][CH:19]=[CH:20][CH:21]=1)[C:25]([OH:27])=[O:26]

Participants

5

Reactant 4

HCID 40755-Aminosalicylic AcidHCID 5339Sulfasalazine2×HCID 22419OlsalazineHCID 545855-({4-[(2-Carboxyethyl)carbamoyl]phenyl}diazenyl)-2-hydroxybenzoic acid

Product 1

HCID 16051978HCID 16051978, compound

Procedure

sulfasalazine, mesalazine, olsalazine, balsalazide, salazosulfapyridine.

Sources & evidence

ORD record
ord-442d9fd5213e45e6910ecc261b807437
Source dataset
uspto-grants-2016_06
Patent number
US09365520B2

Linked notes

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