Hydrochloric Acid → (R)-1-(7-azido-1,2,7,8,9,10-hexahydrobenzo[f]isoquinolin-3(4H)-yl)-2,2,2-trifluoroethanone
Reaction equation
[F:1][C:2]([F:21])([F:20])[C:3]([N:5]1[CH2:14][CH2:13][C:12]2[C:11]3[CH2:15][CH2:16][CH2:17][C@H:18](O)[C:10]=3[CH:9]=[CH:8][C:7]=2[CH2:6]1)=[O:4].C1C=CC(P([N:36]=[N+:37]=[N-:38])(C2C=CC=CC=2)=O)=CC=1.C1CCN2C(=NCCC2)CC1.Cl>C1(C)C=CC=CC=1>[N:36]([C@H:18]1[C:10]2[CH:9]=[CH:8][C:7]3[CH2:6][N:5]([C:3](=[O:4])[C:2]([F:21])([F:20])[F:1])[CH2:14][CH2:13][C:12]=3[C:11]=2[CH2:15][CH2:16][CH2:17]1)=[N+:37]=[N-:38]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of (S)-2,2,2-trifluoro-1-(7-hydroxy-1,2,7,8,9,10-hexahydrobenzo[f]isoquinolin-3(4H)-yl)ethanone (299 mg, 1 mmol) in 3 mL of toluene at −10° C. was added DPPA (0.26 mL, 1.2 mmol). To this stirred solution was then added DBU (0.18 mL, 1.2 mmol) dropwise while keeping the temperature below 0° C. After stirring at room temperature for 3 h, 0.5 mL of 10% HCl was added and the resulting solution was evaporated to dryness and directly submitted to flash chomatography (SiO2, hexane/EtOAc=100:10 to 100:15 to 100:18) to afford (R)-1-(7-azido-1,2,7,8,9,10-hexahydrobenzo[f]-isoquinolin-3(4H)-yl)-2,2,2-trifluoroethanone as a colorless oil which was directly used in the next step.
Workup
- customthe temperature below 0° C
- customthe resulting solution was evaporated to dryness
Sources & evidence
- ORD record
- ord-98bb3274ade6487ab6f3e85d3a8f4ac4
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07662811B2
Reaction notes
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