HCID 12011832, compound → HCID 12011831, compound

HRID 1814269Notes

Reaction equation

HRID 1814269 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[CH:4][C:3]=1[C:9]1[S:10][CH:11]=[C:12](C)[N:13]=1.NC1C=CC(N)=CC=1C1SC(C)=CN=1.NC1C=CC(N)=CC=1C1SC=C(Cl)N=1.NC1C=CC(N)=CC=1C1SC(Cl)=CN=1.NC1C=CC(N)=CC=1C1SC([N+]([O-])=O)=CN=1.NC1C=CC(N)=CC=1C1SC(C)=C(C)N=1.NC1C=CC(N)=CC=1C1SC(CCO)=C(C)N=1.NC1C=CC(N)=CC=1C1SC=C(C2C=CC=CC=2)N=1.NC1C=CC(N)=CC=1C1SC(C2C=CC=CC=2)=CN=1.NC1C=CC(NC)=CC=1C1SC=CN=1.NC1C=CC(NCCO)=CC=1C1SC=CN=1.NC1C=CC(N(CCO)CCO)=CC=1C1SC=CN=1>>[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:8])=[CH:4][C:3]=1[C:9]1[S:10][CH:11]=[CH:12][N:13]=1

Participants

13

Reactant 12

HCID 12011832HCID 12011832, compoundHCID 12011833HCID 12011833, compoundHCID 12011834HCID 12011834, compoundHCID 22506045HCID 22506045, compoundHCID 22506046HCID 22506046, compound2×HCID 22506047HCID 22506047, compoundHCID 22506048HCID 22506048, compoundHCID 22506049HCID 22506049, compoundHCID 22506051HCID 22506051, compoundHCID 22506052HCID 22506052, compoundHCID 22506053HCID 22506053, compoundHCID 22506054HCID 22506054, compound

Product 1

HCID 12011831HCID 12011831, compound

Procedure

1,4-diamino-2-(4-methylthiazol-2-yl)benzene; 1,4-diamino-2-(5-methylthiazol-2-yl)benzene; 1,4-diamino-2-(4-chlorothiazol-2-yl)-benzene; 1,4-diamino-2-(5-chlorothiazol-2-yl)benzene; 1,4-diamino-2-(5-nitrothiazol-2-yl)benzene; 1,4-diamino-2-(4,5-dimethylthiazol-2-yl)benzene; 1,4-diamino-2-[4-methyl-5-(2-hydroxyethyl)thiazol-2-yl]benzene; 1,4-diamino-2-(4-phenylthiazol-2-yl)-benzene; 1,4-diamino-2-(5-nitrothiazol-2-yl)benzene; 1,4-diamino-2-(5-phenylthiazol-2-yl)benzene; 1-amino-4-methylamino-2-(thiazol-2-yl)benzene; 1-amino-4-(2-hydroxyethyl)amino-2-(thiazol-2-yl)benzene and 1-amino-4-bis(2-hydroxyethyl)amino-2-(thiazol-2-yl)benzene.

Sources & evidence

ORD record
ord-1aa40edc423547d1867ab34169765bff
Source dataset
uspto-grants-2005_04
Patent number
US06875873B2

Reaction notes

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