Thiourea → HCID 178419272, compound

HRID 1758734Notes

Reaction equation

HRID 1758734 reaction equation
[BrH:1].[Br:2][CH2:3][C:4]([C:6]1[N:7]=[C:8]([NH:11][C:12]([NH2:14])=[NH:13])[S:9][CH:10]=1)=O.[NH2:15][C:16]([NH2:18])=[S:17]>CN(C)C=O>[BrH:2].[BrH:1].[NH:11]([C:8]1[S:9][CH:10]=[C:6]([C:4]2[N:15]=[C:16]([NH2:18])[S:17][CH:3]=2)[N:7]=1)[C:12]([NH2:14])=[NH:13]

Participants

4

Reactant 2

HCID 2723790ThioureaHCID 178419719HCID 178419719, compound

Product 1

HCID 178419272HCID 178419272, compoundYield 74%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

A solution of 688 mg (2.0 mmol) of 2-bromo-1-(2-guanidino-4-thiazolyl)ethanone hydrobromide and 183 mg of thiourea in 5 ml of dimethylformamide was stirred at room temperature. After a short time, a solid began to precipitate. After a total of four hours, the solid was collected by filtration, washed with ethyl acetate, and dried, thereby affording 595 mg (74%) of 2-guanidino-4-(2-amino-4-thiazolyl)thiazole dihydrobromide as a white powder; mp 320° (dec); mass spectrum parent of 240. This material could be converted to its free base by triturating with saturated sodium bicarbonate solution, stirring for 15 minutes, filtering the solid, and drying it under vacuum. In this way 2-guanidino-4-(2-amino-4-thiazolyl)thiazole was obtained as a crystalline solid, mp 274°. Calcd. for C7H8N6S2 : C, 34.99; H, 3.36; N, 34.97; found: C, 34.94; H, 3.41; N, 34.80.

Workup

  1. customto precipitate
  2. filtrationAfter a total of four hours, the solid was collected by filtration
  3. washwashed with ethyl acetate
  4. customdried

Sources & evidence

ORD record
ord-b3cc0df8a9dd45b29f8889a48e9153bd
Source dataset
uspto-grants-1983_02
Patent number
US04374843

Reaction notes

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