Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 178511596 | HCID 178511596 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 178505709 | HCID 178505709 | 30.2% |
Reaction Steps
To trans-N1-(4-(6-(3-fluorobenzyl amino)pyrazin-2-yl)pyridin-2-yl)cyclohexane-1,4-diamine (19 mg, 0.048 mmol) was added NMP (0.6 ml), acetic acid (0.042 ml, 0.726 mmol) and benzaldehyde (10.27 mg, 0.097 mmol). The resulting reaction mixture was stirred overnight at ambient temperature. To the srirred reaction mixture was added sodium triacetoxyborohydride (41.0 mg, 0.194 mmol) and the resulting mixture was stirred overnight (24 hours) at ambient temperature. To the reaction mixture mixture then was added additional sodium triacetoxyborohydride (21.0 mg, 0.099 mmol) and the resulting mixture was stirred for an additional 2 more hours. To the crude mixture then was added 0.8 ml of DMSO, filtered and purified by prep LC. After lyophilization, 7.0 mg of the title compound was obtained as a TFA salt. LCMS (m/z): 483.2 (MH+), retention time=0.65 min.; 1H NMR (300 MHz, METHANOL-d4, 25° C.) δ ppm 1.35-1.51 (m, 2 H) 1.51-1.69 (m, 2 H) 2.04-2.36 (m, 4 H) 3.08-3.18 (m, 1 H) 3.56-3.70 (m, 1 H) 4.16 (s, 2 H) 4.60 (s, 2 H) 6.82-6.93 (m, 1 H) 7.03 (d, J=9.67 Hz, 1 H) 7.11 (d, J=7.62 Hz, 1 H) 7.19-7.29 (m, 1 H) 7.32 (d, J=6.74 Hz, 1 H) 7.35-7.46 (m, 5 H) 7.54 (s, 1 H) 7.80 (d, J=6.74 Hz, 1 H) 7.97 (s, 1 H) 8.25 (s, 1 H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415381B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-8f77ddc4a94c4ed79ffa83ad66f4fbe9 |
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| Source note | uspto-grants-2013_04 |
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