Water → HCID 68690353, compound

HRID 1296316Notes

Reaction equation

HRID 1296316 reaction equation
[CH2:1]([N:8]1[CH2:23][CH2:22][N:11]2[C:12](=[O:21])[C:13]3[CH:14]=[C:15](Br)[CH:16]=[CH:17][C:18]=3[CH2:19][C@@H:10]2[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:24]([Cu])#[N:25].CCOC(C)=O.O>CN1CCN(C)C1=O.[Cu]I>[CH2:1]([N:8]1[CH2:23][CH2:22][N:11]2[C:12](=[O:21])[C:13]3[CH:14]=[C:15]([C:24]#[N:25])[CH:16]=[CH:17][C:18]=3[CH2:19][C@@H:10]2[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

7

Conditions

Temperature
190 °C

Procedure

Mixture of (R)-2-Benzyl-8-bromo-1,2,3,4,11,11a-hexahydro-pyrazino[1,2-b]isoquinolin-6-one (25 mg, 0.067 mmol), CuCN (12.9 mg, 0.14 mmol) and CuI (3.7 mg, 0.29 mmol) in 1,3-dimethyl-2-imidazolidinone (1.5 mL) was stirred at 190° C. for 83 min in microwave. The reaction was cooled to RT and added EtOAc (20 mL) and H2O (5 mL). Filtered off the precipitate and rinsed with EtOAc (50 mL). The organic layer was separated and washed with brine (5 mL), dried over MgSO4, and conc in vacuo to give crude product. Purified by prep TLC (SiO2, 95:5, CH2Cl2:MeOH) to yield crude product as a yellow oil. MS (ESI) 318 (M+H).

Workup

  1. temperatureThe reaction was cooled to RT
  2. filtrationFiltered off the precipitate
  3. washrinsed with EtOAc (50 mL)
  4. customThe organic layer was separated
  5. washwashed with brine (5 mL)
  6. dry with materialdried over MgSO4
  7. customconc in vacuo to give crude product
  8. customPurified by prep TLC (SiO2, 95:5, CH2Cl2:MeOH)
  9. customto yield crude product as a yellow oil

Sources & evidence

ORD record
ord-e0e99540f24b45f99205e36b7d03752c
Source dataset
uspto-grants-2007_07
Patent number
US07244843B2

Reaction notes

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