Hydrochloric Acid → 1-Methyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole
Reaction equation
[CH3:1][N:2]1[C:6]2[CH2:7][N:8](C(C3C=CC=CC=3)(C3C=CC=CC=3)C3C=CC=CC=3)[CH2:9][C:5]=2[CH:4]=[N:3]1.Cl>>[CH3:1][N:2]1[C:6]2[CH2:7][NH:8][CH2:9][C:5]=2[CH:4]=[N:3]1Participants
3
Procedure
1-Methyl-5-trityl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole (670 mg) obtained in Step A above was treated with 4N hydrochloric acid (4 mL). After 1.5 h, the reaction mixture was concentrated. The residue was purified on a Biotage Horizon® system (silica, gradient 10-19% methanol containing 10% concentrated ammonium hydroxide in dichloromethane) to yield 1-methyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole. LC-MS 124.1 (M+1).
Workup
- concentrationthe reaction mixture was concentrated
- customThe residue was purified on a Biotage Horizon® system (silica, gradient 10-19% methanol containing 10% concentrated ammonium hydroxide in dichloromethane)
Sources & evidence
- ORD record
- ord-7ae6ec1bd35a4db0907eb1e6cd8a96be
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07678905B2
Reaction notes
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