Sodium Nitrite → HCID 53734507, compound
Reaction equation
[Cl:1][CH2:2][CH2:3][NH:4][C:5]([N:7]([CH2:19][CH2:20][CH2:21][CH3:22])[CH:8]1[O:16][C@H:15]([CH2:17][OH:18])[C@H:13]([OH:14])[C@H:11]([OH:12])[C@H:9]1[OH:10])=[O:6].[N:23]([O-])=[O:24].[Na+]>C(O)=O>[Cl:1][CH2:2][CH2:3][N:4]([N:23]=[O:24])[C:5]([N:7]([CH2:19][CH2:20][CH2:21][CH3:22])[CH:8]1[O:16][C@H:15]([CH2:17][OH:18])[C@H:13]([OH:14])[C@H:11]([OH:12])[C@H:9]1[OH:10])=[O:6]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4.8 g of 1-(2-chloroethyl)-3-n-butyl-3-D-galactopyranosylurea are dissolved in 15 ml of formic acid, and 2.4 g of sodium nitrite are added gradually thereto at 0° to 5° C. for one hour under stirring. The mixture is further stirred at the same temperature for 1.5 hours. After the reaction, the mixture is treated in the same manner as described in Example 5-(2). 1.8 g of 1-(2-chloroethyl)-1-nitroso-3-n-butyl-3-D-galactopyranosylurea are thereby obtained as a yellow powder.
Workup
- stirringThe mixture is further stirred at the same temperature for 1.5 hours
- customAfter the reaction
- additionthe mixture is treated in the same manner
Sources & evidence
- ORD record
- ord-58fa17e16c1b49a08d7a964cd32d2886
- Source dataset
- uspto-grants-1980_01
- Patent number
- US04182757
Reaction notes
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