Hydrochloric Acid → HCID 75204201, compound
Reaction equation
[C:1]1([N:10]2[CH2:14][CH2:13][C@H:12]([NH:15]C(=O)OC(C)(C)C)[CH2:11]2)[C:2]2[N:3]([CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:5][N:6]=1.Cl>O1CCOCC1>[C:1]1([N:10]2[CH2:14][CH2:13][C@H:12]([NH2:15])[CH2:11]2)[C:2]2[N:3]([CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:5][N:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
To a solution of (S)-tert-butyl N-(1-(pyrrolo[1,2-a]pyrazin-1-yl)pyrrolidin-3-yl)carbamate (0.88 g, 2.9 mmol, 1 eq) in 3.6 mL of dioxane was added a solution of 4.0 M HCl in dioxane (3.6 mL, 14.5 mmol, 5 eq). After heating for 1 h at 60° C., the mixture was concentrated to afford (S)-1-(pyrrolo[1,2-a]pyrazin-1-yl)pyrrolidin-3-amine (0.79 g, 2.9 mmol, 100%).
Workup
- concentrationthe mixture was concentrated
Sources & evidence
- ORD record
- ord-97480de863aa4b918a29e65a4c7b0032
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09169261B2
Reaction notes
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