Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 3-carbamoyl-4-chloropyrrolo[1,2-b]pyridazine-6-carboxylate | HCID 68290691 | — |
| Product | HCID 68349556 | HCID 68349556 | 81% |
Reaction Steps
A solution of ethyl 3-carbamoyl-4-chloropyrrolo[1,2-b]pyridazine-6-carboxylate (1.25 g, 4.67 mmol) (R)-1-(1-methylcyclopropyl)ethanamine (0.697 g, 5.14 mmol) and DIPEA (2.039 mL, 11.67 mmol) in NMP (Volume: 5 mL) was heated to 100° C. for 4 hr. The reaction mixture was added 100 mL of EtOAc which was washed with 50 mL of water, 50 mL of 10% LiCl solution and 50 mL of brine, dried over Na2SO4. Filtration and concentration to yield a crude product which was purified on silica gel column with hexanes/EtOAc(1/1) to yield the desired product (1.246 g, 81% yield). 1H NMR (400 MHz, CD3OD) δ 8.23 (s, 1H), 8.03 (d, J=1.8 Hz, 1H), 7.32 (d, J=1.8 Hz, 1H), 4.38 (d, J=7.0 Hz, 2H), 4.04-3.93 (m, 1H), 1.46-1.36 (m, 6H), 1.27 (s, 3H), 0.65-0.51 (m, 2H), 0.48-0.37 (m, 2H). MS (ES+) m/z: 331.08 (M+H); HPLC: 96%, retention time: 3.260 min (analytical HPLC Method B).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221826B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-192d07553e6f4c5596a27fdd938c9515 |
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| Source note | uspto-grants-2015_12 |
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