Sodium borohydride → HCID 178512085, compound
Reaction equation
[BH4-].[Na+].[CH2:3]1[O:11][C:10]2[CH:9]=[CH:8][C:7]([C:12](=[O:32])[CH2:13][N:14]3[CH2:19][CH2:18][CH:17]([N:20]4[C:24]5[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=5[NH:22][C:21]4=[N:29][C:30]#[N:31])[CH2:16][CH2:15]3)=[CH:6][C:5]=2[O:4]1>C(O)C>[CH2:3]1[O:11][C:10]2[CH:9]=[CH:8][C:7]([CH:12]([OH:32])[CH2:13][N:14]3[CH2:19][CH2:18][CH:17]([N:20]4[C:24]5[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=5[NH:22][C:21]4=[N:29][C:30]#[N:31])[CH2:16][CH2:15]3)=[CH:6][C:5]=2[O:4]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In this example, 600 mg of sodium borohydride is added to a suspension of 715 mg of the product obtained in Example 9 in 30 ml of ethanol at room temperature. After completion of the addition, the reaction mixture is concentrated. The residue is mixed with water, and the crystals deposited are separated by filtration and dried. The crude crystals are recrystallized from methanol to obtain 632 mg of the desired product.
Workup
- additionAfter completion of the addition
- concentrationthe reaction mixture is concentrated
- additionThe residue is mixed with water
- customthe crystals deposited are separated by filtration
- customdried
- customThe crude crystals are recrystallized from methanol
Sources & evidence
- ORD record
- ord-3061a33aaa9642f4b6ff5fbfe272ae88
- Source dataset
- uspto-grants-1983_10
- Patent number
- US04410528
Reaction notes
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