Sodium Bicarbonate → 2-Guanidino-4-(2-hydroxymethyl-4-imidazolyl)thiazole hydrobromide
Reaction equation
Br.[OH:2][CH2:3][C:4]1[NH:5][CH:6]=[C:7]([C:9](=O)[CH2:10][Br:11])[N:8]=1.C(=O)(O)[O-].[Na+].[C:18]([NH:21][C:22]([NH2:24])=[S:23])(=[NH:20])[NH2:19]>O.CC(C)=O>[BrH:11].[NH:21]([C:22]1[S:23][CH:10]=[C:9]([C:7]2[N:8]=[C:4]([CH2:3][OH:2])[NH:5][CH:6]=2)[N:24]=1)[C:18]([NH2:20])=[NH:19]Participants
Procedure
1.78 g (0.0059 mol) of 2-hydroxymethyl-4-bromoacetylimidazole hydrobromide was dissolved in water and saturated sodium bicarbonate solution was added to precipitate the free base. This material was collected by filtration and dried and combined with 956 mg (0.0081 mol) of amidinothiourea in 60 ml acetone and heated to 70° . After 15 minutes heating a solid formed. The reaction mixture was cooled and the resultant solid was collected by filtration to give 1.65 g (87%) 2-guanidino-4-(2-hydroxymethyl-4-imidazolyl)thiazole hydrobromide, mp>310°. A sample was converted to the free base by dissolving in hot water and adding sodium bicarbonate solid to pH 10 to precipitate 2-guanidino-4-(2-hydroxymethyl-4-imidazolyl)thiazole free base. This material was dried over toluene at high vacuum to give a light tan solid, mp 208°-209° with decomposition. nmr (DMSO-d6) (δ): 7.16 (s, 1H); 6.83 (broad s, 4H) 6.68 (s, 1H); 4.45 (s, 2H); 3.46 (very broad s, 1H). High resolution mass spectrum, calcd for C8H10N6OS: 238.0638; found: 238.0654.
Workup
- customto precipitate the free base
- filtrationThis material was collected by filtration
- customdried
- temperatureheated to 70°
- temperatureAfter 15 minutes heating a solid
- customformed
- temperatureThe reaction mixture was cooled
- filtrationthe resultant solid was collected by filtration
Sources & evidence
- ORD record
- ord-d8c024e2c82e417db9c76ee7fc064390
- Source dataset
- uspto-grants-1986_05
- Patent number
- US04590299
Reaction notes
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