Hydrochloric Acid → Cytarabine Hydrochloride
Reaction equation
[CH:1]1[C:7]([NH2:8])=[N:6][C:4](=[O:5])[N:3]([C@@H:9]2[O:13][C@H:12]([CH2:14][OH:15])[C@@H:11]([OH:16])[C@@H:10]2[OH:17])[CH:2]=1.[ClH:18]>CO>[CH:1]1[C:7]([NH2:8])=[N:6][C:4](=[O:5])[N:3]([C@@H:9]2[O:13][C@H:12]([CH2:14][OH:15])[C@@H:11]([OH:16])[C@@H:10]2[OH:17])[CH:2]=1.[ClH:18]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 2 °C
Procedure
A 5 L, 3-neck flask equipped with an overhead stirrer and thermocouple was charged with cytarabine (500 g, 2.06 mol) and methanol (2.0 L). The suspension was cooled to 2° C. HCl gas was bubbled in, giving a very thick mixture and an exotherm to 25° C. The suspension was diluted with methanol (0.5 L) to facilitate stirring. A total of 108 g (2.96 mol) of HCl gas was added. The mixture was stirred for 4 hours at 20° C. then filtered to collect the solid. The solid was washed with MTBE (3×250 mL) and dried in a vacuum oven at 70° C. to give 555 g (96% yield) of cytarabine hydrochloride as a flocculent, white solid.
Workup
- customA 5 L, 3-neck flask equipped with an overhead stirrer
- customHCl gas was bubbled in,
- customgiving a very thick mixture
- customto 25° C
- stirringThe mixture was stirred for 4 hours at 20° C.
- filtrationthen filtered
- customto collect the solid
- washThe solid was washed with MTBE (3×250 mL)
- customdried in a vacuum oven at 70° C.
Sources & evidence
- ORD record
- ord-e8283582e54f4892a69fd5f201a4c969
- Source dataset
- uspto-grants-2009_03
- Patent number
- US07498320B2
Reaction notes
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