Citric Acid → Tofacitinib Citrate

HRID 1716267Notes

Reaction equation

HRID 1716267 reaction equation
[CH3:1][C@@H:2]1[CH2:7][CH2:6][N:5]([C:8](=[O:12])[CH2:9][C:10]#[N:11])[CH2:4][C@@H:3]1[N:13]([CH3:23])[C:14]1[C:15]2[CH:22]=[CH:21][NH:20][C:16]=2[N:17]=[CH:18][N:19]=1.[C:24]([OH:36])(=[O:35])[CH2:25][C:26]([CH2:31][C:32]([OH:34])=[O:33])([C:28]([OH:30])=[O:29])[OH:27]>CC(C)=O>[C:24]([OH:36])(=[O:35])[CH2:25][C:26]([CH2:31][C:32]([OH:34])=[O:33])([C:28]([OH:30])=[O:29])[OH:27].[CH3:1][C@@H:2]1[CH2:7][CH2:6][N:5]([C:8](=[O:12])[CH2:9][C:10]#[N:11])[CH2:4][C@@H:3]1[N:13]([CH3:23])[C:14]1[C:15]2[CH:22]=[CH:21][NH:20][C:16]=2[N:17]=[CH:18][N:19]=1

Participants

4

Conditions

Temperature
40 °C

Procedure

A stirred solution of (3R,4R)-3-{4-Methyl-3-[methyl-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-amino]-piperidin-1-yl}-3-oxo-propionitrile (230 mg/0.74 mmol) dissolved in 23 mL of acetone was heated to 40° C. To this solution was added 155 mg (0.81 mmol) of finely ground citric acid. The resulting mixture stirred at 40° C. for 2 hours, then at 30° C. for 4 hours followed by stirring at room temperature for an additional 18 hours. At this point, the solids were collected by filtration, washed with acetone and dried in vacuo affording 280 mg (75%) of the title compound as a white crystalline solid.

Workup

  1. waitat 30° C. for 4 hours followed
  2. stirringby stirring at room temperature for an additional 18 hours
  3. filtrationAt this point, the solids were collected by filtration
  4. washwashed with acetone
  5. customdried in vacuo

Sources & evidence

ORD record
ord-3c38a444888a4c8fa52afb1d11e3b490
Source dataset
uspto-grants-2010_09
Patent number
US07803805B2

Reaction notes

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