HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → HCID 71496052, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | HCID 71496163 | HCID 71496163 | — |
| Reactant | HCID 71496699 | HCID 71496699 | — |
| Product | HCID 71496052 | HCID 71496052 | 64.4% |
Reaction Steps
The title compound was prepared in the same manner as in Example 21, with the exception that (S)—N-(3-chlorophenyl)-2-(3-piperidylamino)nicotinamide of Example 20-A, instead of N-(3-chlorophenyl)-2-(2,2,6,6-tetramethylpiperidin-4-ylamino)nicotinamide, and benzylchloride, instead of 2-bromoethanol, were used in the same molar amounts (Yield: 64.4%). 1H NMR (CDCl3) δ 8.33 (d, 1H), 8.24 (d, 1H), 7.83 (s, 1H), 7.74 (s, 1H), 7.68 (d, 1H), 7.47-7.13 (m, 7H), 6.53-6.46 (m, 1H), 4.39-4.27 (m, 1H), 2.69 (d, 1H), 2.53-2.34 (m, 3H), 1.85-1.58 (m, 6H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09227955B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-0659c7ed79f946008644c11ed9ceee7b |
| Source note | uspto-grants-2016_01 |