HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 131732908, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | L-Tartaric acid | HCID 444305 | — |
| Reactant | HCID 56847761 | HCID 56847761 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131732908 | HCID 131732908 | 0.1% |
Reaction Steps
To the product from Step B (19 mg, 43 mmol) acetonitrile (0.5 mL) was added L-tartaric acid (6.5 mg, 43 mmol) in water (2 mL). The resultant solution was lyophilized for 48 hours to give 6-(5-(3-chloro-4-fluorophenyl)-1,3,4,5-tetrahydro-2,5-ethanobenzo[c]azepin-8-yl)-N-methylpyridazine-3-carboxamide, L-tartrate salt (22 mg, 98%, HPLC: 98.8%) as an off-white solid: 1H NMR (400 MHz, CD3OD): δ 8.32 (m, 2H), 8.16 (s, 1H), 7.91 (d, J=8.0 Hz, 1H), 7.53 (d, J=7.2 Hz, 1H), 7.37 (m, 2H), 6.62 (d, J=8.4 Hz, 1H), 4.95 (m, 2H), 4.46 (s, 2H), 3.65-3.34 (m, 4H), 3.06 (s, 3H), 2.84 (m, 2H), 2.50 (m, 2H). ESI MS (m/z): 437 [M′+1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045468B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-2c1d5606826147ea9ea6cb4139660120 |
| Source note | uspto-grants-2015_06 |