Dimethylamine → HCID 68283791, compound
Reaction equation
Cl[C:2]([C:22]1[CH:27]=[N:26][CH:25]=[CH:24][N:23]=1)([CH3:21])[CH2:3][N:4]1[C:16]2[CH2:15][CH2:14][N:13]3[CH2:17][CH2:18][CH2:19][CH:12]3[C:11]=2[C:10]2[CH:9]=[C:8]([CH3:20])[CH:7]=[CH:6][C:5]1=2.[CH3:28][NH:29][CH3:30]>O>[CH3:28][N:29]([CH3:30])[C:2]([CH3:21])([C:22]1[CH:27]=[N:26][CH:25]=[CH:24][N:23]=1)[CH2:3][N:4]1[C:16]2[CH2:15][CH2:14][N:13]3[CH2:17][CH2:18][CH2:19][CH:12]3[C:11]=2[C:10]2[CH:9]=[C:8]([CH3:20])[CH:7]=[CH:6][C:5]1=2Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
6-(2-Chloro-2-pyrazin-2-yl-propyl)-9-methyl-2,3,4,5,6,10c-hexahydro-1H-3a,6-diaza-cyclopenta[c]fluorene (500 mg, 1.31 mmol) in 40% dimethylamine in water (30 mL) was heated at 100° C. for 3 h. The reaction mixture was cooled at RT and extracted with EtOAc (3×50 mL). The combined organic layer was dried over anhydrous sodium sulfate and concentrated to obtain the crude product, which was purified by reverse phase chromatography to obtain 62 mg of dimethyl-[1-methyl-2-(9-methyl-1,2,3,4,5,10c-hexahydro-3a,6-diaza-cyclopenta[c]fluoren-6-yl)-1-pyrazin-2-yl-ethyl]-amine. 1H NMR (CD3OD, TFA salt): δ (ppm): 8.06 (s, 1H), 7.48 (s, 1H), 7.21 (s, 1H), 7.17 (d, 1H), 7.00 (d, 1H), 4.98 (t, 1H), 4.28 (d, 2H), 3.6 (m, 3H), 3.39 (m, 2H), 3.2 (m, 1H), 3.15 (s, 6H), 2.8 (m, 1H), 2.7 (m, 1H), 2.39 (s, 3H), 2.17 (m, 3H). Chiral HPLC separated the racemate into diastereomers II-6a-d.
Workup
- extractionextracted with EtOAc (3×50 mL)
- dry with materialThe combined organic layer was dried over anhydrous sodium sulfate
- concentrationconcentrated
- customto obtain the crude product, which
- customwas purified by reverse phase chromatography
Sources & evidence
- ORD record
- ord-9372ae76da584783a3c4e622ee1a1c4b
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09006263B2
Reaction notes
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