Sodium Bicarbonate → HCID 22760515, compound
Reaction equation
Br.[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2([OH:22])[CH2:13][S:12][C:11](=[N:14][CH2:15][CH:16]3[CH2:20][CH2:19][CH2:18][CH2:17]3)[N:10]2[CH3:21])=[CH:5][C:4]=1[S:23](=[O:26])(=[O:25])[NH2:24].C(=O)(O)[O-].[Na+]>>[Cl:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2([OH:22])[CH2:13][S:12][C:11](=[N:14][CH2:15][CH:16]3[CH2:20][CH2:19][CH2:18][CH2:17]3)[N:10]2[CH3:21])=[CH:5][C:4]=1[S:23](=[O:25])(=[O:26])[NH2:24]Participants
3
Procedure
6 g of 4-(4-chloro-3-sulfamoylphenyl)-2-cyclopentylmethylimino-3-methyl-1,3-thiazolidine-4-ol-hydrobromide were reacted according to the prescription given in Example 2(c) with sodium bicarbonate. Colorless solid body: decomposition beginning at 115° C. γC=N 1615 cm-1.
Workup
- custombeginning at 115° C.
Sources & evidence
- ORD record
- ord-d612691ffdeb4652b4a5a72df1ffbf71
- Source dataset
- uspto-grants-1978_11
- Patent number
- US04125614
Reaction notes
Loading…