HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 57560985, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 2-Cyclopropyl-2-hydroxyacetonitrile | HCID 11389359 | — |
| Reactant | HCID 67273084 | HCID 67273084 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57560985 | HCID 57560985 | 50% |
Reaction Steps
To the suspension of N-(2-azabicyclo[2.2.1]hept-5-yl)-1H-indazole-3-carboxamide hydrochloride (0.36 mmol), cyclopropylcarboxaldehyde (0.9 mmol), and N,N-diisopropylethylamine (1.08 mmol), acetic acid (0.43 mmol) was added sodium triacetoxyborohydride (0.61 mmol). The reaction mixture was maintained at rt for 2 h and was poured into water, extracted with 95/5 dichloromethane/methanol (2×30 mL), and the combined extracts were concentrated. The residue was purified by preparative HPLC, thus providing the product in 50% yield. 1H NMR (CD3OD) δ 8.21 (m, 1H), 7.59 (m, 1H), 7.45 (m, 1H), 7.26 (m, 1H), 4.15 (m, 1H), 3.83 (m, 1H), 3.10 (m, 3H), 2.02 (m, 4H), 1.37 (m, 2H), 0.74 (m, 2H), 0.48 (m, 2H); LC/MS (EI) tR 2.72 min, m/z 311 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902217B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-3cb8a5a2ffb14903856bf828ee5cee20 |
| Source note | uspto-grants-2011_03 |