HCID 178438357, compound → HCID 178435439, compound

HRID 441655Notes

Reaction equation

HRID 441655 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]([CH2:23][CH2:24]C)[C:20]([CH2:26][CH2:27]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(C(C)C)C(C(C)C)=CC=43)=NC=2)=O)=NN=N1.N1C(NC(C2C(=O)N3C(SC4C=C(CCC)C(C)=CC=43)=NC=2)=O)=NN=N1.N1C(NC(C2C(=O)N3C(SC4C=C(C)C(CCC)=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]([CH2:23][CH3:24])[C:20]([CH2:26][CH3:27])=[CH:19][C:15]=43)=[N:11][CH:10]=2)=[O:8])=[N:4][N:3]=[N:2]1

Participants

5

Reactant 4

HCID 178438357HCID 178438357, compoundHCID 178438407HCID 178438407, compoundHCID 178438408HCID 178438408, compoundHCID 178438409HCID 178438409, compound

Product 1

HCID 178435439HCID 178435439, compound

Procedure

N-(5-tetrazolyl)-7,8-di-n-propyl-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide; N-(5-tetrazolyl)-7,8-di-i-propyl-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide; N-(5-tetrazolyl)-7-methyl-8-n-propyl-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide; and N-(5-tetrazolyl)-7-n-propyl-8-methyl-4-oxo-4H-pyrimido[2,1-b]benzothiazole-3-carboxamide.

Sources & evidence

ORD record
ord-08fb9f94d99f4ca0a104d7cc075b4df0
Source dataset
uspto-grants-1977_08
Patent number
US04041163

Reaction notes

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