Dichloromethane → 2-{4'-[(3Ar,6ar)-5-methylhexahydropyrrolo[3,4-b]pyrrol-1(2h)-yl]-1,1'-biphenyl-4-yl}pyridazin-3(2h)-one l-tartrate salt monohydrate

HRID 12985Notes

Reaction equation

HRID 12985 reaction equation
[C:1]([CH:4]([CH:6]([C:8]([OH:10])=[O:9])[OH:7])[OH:5])([OH:3])=[O:2].[CH3:11][N:12]1[CH2:19][C@@H:18]2[C@@H:14]([N:15]([C:20]3[CH:25]=[CH:24][C:23]([C:26]4[CH:31]=[CH:30][C:29]([N:32]5[C:37](=[O:38])[CH:36]=[CH:35][CH:34]=[N:33]5)=[CH:28][CH:27]=4)=[CH:22][CH:21]=3)[CH2:16][CH2:17]2)[CH2:13]1.ClCCl>O>[OH2:2].[C:1]([C@@H:4]([C@H:6]([C:8]([OH:10])=[O:9])[OH:7])[OH:5])([OH:3])=[O:2].[CH3:11][N:12]1[CH2:19][C@@H:18]2[C@@H:14]([N:15]([C:20]3[CH:25]=[CH:24][C:23]([C:26]4[CH:31]=[CH:30][C:29]([N:32]5[C:37](=[O:38])[CH:36]=[CH:35][CH:34]=[N:33]5)=[CH:28][CH:27]=4)=[CH:22][CH:21]=3)[CH2:16][CH2:17]2)[CH2:13]1

Participants

4

Conditions

Temperature
40 °C

Procedure

2-{4′-[(3aR,6aR)-5-Methylhexahydropyrrolo[3,4-b]pyrrol-1(2H)-yl]-1,1′-biphenyl-4-yl}pyridazin-3(2H)-one tartrate (Form A) was suspended in 1 mL of solution mixture, which was prepared by mixing 3.0 mL of dichloromethane with 1.5 mL of 20% water (in methanol). The suspension was vortexed and heated in a shaking water bath to about 40° C. and maintained for 1.5 hrs. It was further heated to about 70° C. The suspension was then filtered. The water bath was turned off, and the supernatant cooled to ambient temperatures naturally in the water bath. Single crystals were offered.

Workup

  1. customwas prepared
  2. temperaturemaintained for 1.5 hrs
  3. temperatureIt was further heated to about 70° C
  4. filtrationThe suspension was then filtered
  5. temperaturethe supernatant cooled to ambient temperatures naturally in the water bath

Sources & evidence

ORD record
ord-8ec567fe6a224eab86469cfeafb1c7e5
Source dataset
uspto-grants-2010_06
Patent number
US07728031B2

Reaction notes

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