Hydrochloric Acid → HCID 11737031, compound
Reaction equation
C(OC([N:8]1[CH2:22][CH2:21][N:11]2[C:12](=[O:20])[C:13]3[C:18]([CH:10]2[CH2:9]1)=[CH:17][CH:16]=[CH:15][C:14]=3[Cl:19])=O)(C)(C)C.Cl>>[ClH:19].[Cl:19][C:14]1[CH:15]=[CH:16][CH:17]=[C:18]2[C:13]=1[C:12](=[O:20])[N:11]1[CH2:21][CH2:22][NH:8][CH2:9][CH:10]12Participants
3
Procedure
To (±)-N-(t-butoxycarbonyl)-1,3,4,10b-tetrahydro-7-chloropyrazino[2,1-a]isoindol-6(2H)-one (15 mg, 0.05 mmol) was added concentrated hydrochloric acid (1 mL). After 15 min, the resulting solution was concentrated, diluted with water, and lyopholized to give (±)-1,3,4,10b-tetrahydro-7-chloro-pyrazino[2,1-a]isoindol-6(2H)-one hydrochloric acid salt as an off-white solid (12 mg, 100%). MS (ESI) 223.2, 225.2 (M−Cl).
Workup
- concentrationthe resulting solution was concentrated
- additiondiluted with water
Sources & evidence
- ORD record
- ord-ddee15f775bf4e168347addeef54547e
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07244843B2
Reaction notes
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