HCID 178438411, compound → HCID 178503069, compound

HRID 441658Notes

Reaction equation

HRID 441658 reaction equation
[NH:1]1[C:5]([NH:6][C:7]([C:9]2[C:17](=[O:18])[N:16]3[C:12]([S:13][C:14]4[CH:22]=[C:21](CCC)[C:20]([N+:26]([O-:28])=[O:27])=[CH:19][C:15]=43)=[N:11][CH:10]=2)=[O:8])=[N:4][N:3]=[N:2]1.N1C(NC(C2C(=O)N3[C:40]([S:41]C4C=C(OC)C([N+]([O-])=O)=CC=43)=NC=2)=O)=NN=N1.N1C(NC(C2C(=O)N3C(SC4C=C(OCC)C([N+]([O-])=O)=CC=43)=NC=2)=O)=NN=N1.N1C(NC(C2C(=O)N3C(SC4C=C(O)C([N+]([O-])=O)=CC=43)=NC=2)=O)=NN=N1.N1C(NC(C2C(=O)N3C(SC4C=C(Cl)C([N+]([O-])=O)=CC=43)=NC=2)=O)=NN=N1.N1C(NC(C2C(=O)N3C(SC4C=C(F)C([N+]([O-])=O)=CC=43)=NC=2)=O)=NN=N1>>[NH:1]1[C:5]([NH:6][C:7]([C:9]2[C:17](=[O:18])[N:16]3[C:12]([S:13][C:14]4[CH:22]=[C:21]([S:41][CH3:40])[C:20]([N+:26]([O-:28])=[O:27])=[CH:19][C:15]=43)=[N:11][CH:10]=2)=[O:8])=[N:4][N:3]=[N:2]1

Participants

7

Reactant 6

HCID 178438411HCID 178438411, compoundHCID 178465857HCID 178465857, compoundHCID 178486930HCID 178486930, compoundHCID 178522708HCID 178522708, compoundHCID 178522714HCID 178522714, compoundHCID 178522715HCID 178522715, compound

Product 1

HCID 178503069HCID 178503069, compound

Procedure

N-(5-tetrazolyl)-7-nitro-8-methyl-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboximide; N-(5-tetrazolyl)-7-nitro-8-n-propyl-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide; N-(5-tetrazolyl)-7-nitro-8-methoxy-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide; N-(5-tetrazolyl)-7-nitro-8-ethoxy-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide; N-(5-tetrazolyl)-7-nitro-8-hydroxy-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide; N-(5-tetrazolyl)-7-nitro-8-chloro-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide; and N-(5-tetrazolyl)-7-nitro-8-fluoro-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide.

Sources & evidence

ORD record
ord-72b5aa606a5040feae1bfe4b30e07518
Source dataset
uspto-grants-1977_08
Patent number
US04041163

Reaction notes

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