HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → HCID 21468666, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 1-Phenethylamine, (-)- | HCID 75818 | — |
| Reactant | HCID 53957623 | HCID 53957623 | — |
| Product | HCID 21468666 | HCID 21468666 | — |
Reaction Steps
The procedure of section (e) can be used generally to prepare many of the amines of formula A-H. For example, by following the latter procedure but replacing (S)-1-phenylethylamine with an equivalent amount of benzylamine, N-methyl-2-[(phenylmethyl)amino]-N-[2-(2 -pyridinyl)ethyl]acetamide was obtained via the corresponding Boc derivative. The Boc derivative had the following NMR: 1H NMR(CDCl3) δ 8.60 (d, J=5 Hz, 1H), 8.40 (m, 1H), 7.70-7.00 (m,7H), 4.55-4.52 and 4.48 (2s,2H), 3.90 (d, J=11 Hz, 1H), 3.80-3.55 (m,2H), 3.10-2.90 (m,3H), 2.90 (s,3H), 1.50 (3s,9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05693619 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-267792569b0b4ad7a710d818780c35c4 |
| Source note | uspto-grants-1997_12 |