HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetonitrile → (4-Pyridin-4-ylmethyl-piperazin-1-yl)-acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | 1-((Pyridin-4-yl)methyl)piperazine | HCID 808715 | — |
| Product | (4-Pyridin-4-ylmethyl-piperazin-1-yl)-acetonitrile | HCID 63337270 | — |
Reaction Steps
The title compound is synthesized by coupling of 1-Pyridin-4-ylmethyl-piperazine (commercially available from ABCR GmbH) and bromoacetonitrile analogously to the preparation of Intermediate 149.2 as a colorless oil; ES-MS: M+=217.2: 1HNMR(CDCl3) 8.55 (d, 2H), 7.25 (d, 2H), 3.50 (s, 4H), 2.70-2.40 (m, 8H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08053457B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-4257399ccb734528a88461f5610ed262 |
| Source note | uspto-grants-2011_11 |