Hydrochloric Acid → Cytarabine Hydrochloride

HRID 1781981Notes

Reaction equation

HRID 1781981 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

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

  1. customA 5 L, 3-neck flask equipped with an overhead stirrer
  2. customHCl gas was bubbled in,
  3. customgiving a very thick mixture
  4. customto 25° C
  5. stirringThe mixture was stirred for 4 hours at 20° C.
  6. filtrationthen filtered
  7. customto collect the solid
  8. washThe solid was washed with MTBE (3×250 mL)
  9. 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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