HCID 178435354, compound → HCID 178503064, compound

HRID 441656Notes

Reaction equation

HRID 441656 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]([S:23][CH3:24])[C:20]([CH2:25]C)=[CH:19][C:15]=43)=[N:11][CH:10]=2)=[O:8])=[N:4][N:3]=[N:2]1.N1C(NC(C2C(=O)N3C(SC4C=C(SC)C(OC)=CC=43)=NC=2)=O)=NN=N1.N1C(NC(C2C(=O)N3C(SC4C=C(SC)C(OCCC)=CC=43)=NC=2)=O)=NN=N1.N1C(NC(C2C(=O)N3C(SC4C=C(SC)C(Cl)=CC=43)=NC=2)=O)=NN=N1.N1C(NC(C2C(=O)N3C(SC4C=C(SC)C(F)=CC=43)=NC=2)=O)=NN=N1.N1C(NC(C2C(=O)N3C(SC4C=C(SC)C(C(F)(F)F)=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:23][CH3:24])[C:20]([CH3:25])=[CH:19][C:15]=43)=[N:11][CH:10]=2)=[O:8])=[N:4][N:3]=[N:2]1

Participants

7

Reactant 6

HCID 178435354HCID 178435354, compoundHCID 178458123HCID 178458123, compoundHCID 178486568HCID 178486568, compoundHCID 178503065HCID 178503065, compoundHCID 178503066HCID 178503066, compoundHCID 178503067HCID 178503067, compound

Product 1

HCID 178503064HCID 178503064, compound

Procedure

N-(5-tetrazolyl)-7-ethyl-8-methylthio-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide; N-(5-tetrazolyl)-7-methoxy-8-methylthio-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide; N-(5-tetrazolyl)-7-n-propoxy-8-methylthio-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide; N-(5-tetrazolyl)-7-chloro-8-methylthio-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide; N-(5-tetrazolyl)-7-fluoro-8-methylthio-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide; and N-(5-tetrazolyl)-7-trifluoromethyl-8-methylthio-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide.

Sources & evidence

ORD record
ord-48363037998346d0a89e8b3652d3fc03
Source dataset
uspto-grants-1977_08
Patent number
US04041163

Reaction notes

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