2-Hydrazinyl-5,6,7,8,9,10-hexahydrocycloocta[d]pyrimidine → N3-(3-fluoro-4-(4-methyl-1,4-diazepan-1-yl)phenyl)-1-(5,6,7,8,9,10-hexahydrocycloocta[d]pyrimidin-2-yl)-1H-1,2,4-triazole-3,5-diamine
Reaction equation
[NH:1]([C:3]1[N:4]=[CH:5][C:6]2[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][C:7]=2[N:8]=1)[NH2:2].[C:15](/[N:17]=[C:18](\OC1C=CC=CC=1)/[NH:19][C:20]1[CH:25]=[CH:24][C:23]([N:26]2[CH2:32][CH2:31][CH2:30][N:29]([CH3:33])[CH2:28][CH2:27]2)=[C:22]([F:34])[CH:21]=1)#[N:16]>CN1CCCC1=O>[F:34][C:22]1[CH:21]=[C:20]([NH:19][C:18]2[N:17]=[C:15]([NH2:16])[N:1]([C:3]3[N:4]=[CH:5][C:6]4[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][C:7]=4[N:8]=3)[N:2]=2)[CH:25]=[CH:24][C:23]=1[N:26]1[CH2:32][CH2:31][CH2:30][N:29]([CH3:33])[CH2:28][CH2:27]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2-Hydrazinyl-5,6,7,8,9,10-hexahydrocycloocta[d]pyrimidine (58 mg, 0.30 mmol) and (Z)-phenyl N′-cyano-N-(3-fluoro-4-(4-methyl-1,4-diazepan-1-yl)phenyl)carbamimidate (111 mg, 0.30 mmol) were dissolved in anhydrous N-methylpyrrolidone (0.5 mL) and subjected to microwave irradiation (220° C., 10 min). The crude reaction mixture was directly purified by C-18 reversed phase chromatography, eluting with acetonitrile and water containing 0.05% formic acid to give N3-(3-fluoro-4-(4-methyl-1,4-diazepan-1-yl)phenyl)-1-(5,6,7,8,9,10-hexahydrocycloocta[d]pyrimidin-2-yl)-1H-1,2,4-triazole-3,5-diamine, compound #4, as a beige solid, 30 mg; 1H NMR (CDCl3/MeOD4, 300 MHz) 8.22 (s, 1H), 8.19 (s, 1H), 7.26 (d, 1H), 6.93 (d, 1H), 6.71 (t, 1H), 3.23 (m, 6H), 3.16 (m, 2H), 2.81 (m, 2H), 2.69 (s, 3H), 2.61 (m, 2H), 2.12 (m, 2H), 1.69 (m, 2H), 1.56 (m, 2H), 1.27 (m, 4H) ppm; MS (ES) 466.27 (M+H).
Workup
- customsubjected to microwave irradiation (220° C., 10 min)
- customThe crude reaction mixture
- customwas directly purified by C-18
- washeluting with acetonitrile and water containing 0.05% formic acid
Sources & evidence
- ORD record
- ord-66f6f28bbf514f45b3be6b42cdf8534b
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08492373B2
Reaction notes
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