HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-allyl-2-hydroxy-3-methoxybenzaldehyde → HCID 136102551, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-allyl-2-hydroxy-3-methoxybenzaldehyde | HCID 1713887 | — |
| Reactant | 6-piperazin-1-yl-3H-pyrimidin-4-one | HCID 136102540 | — |
| Product | HCID 136102551 | HCID 136102551 | — |
Reaction Steps
6-[4-(5-Allyl-2-hydroxy-3-methoxy-benzyl)-piperazin-1-yl]-3H-pyrimidin-4-one was prepared using Procedure B from 6-piperazin-1-yl-3H-pyrimidin-4-one (Intermediate 4) and 5-allyl-2-hydroxy-3-methoxybenzaldehyde (available from Acros Organics, Geel, Belgium). 1H NMR (400 MHz, CDCl3) δ 2.58-2.63 (m, 4H), 3.27-3.29 (m, 2H), 3.58-3.65 (m, 4H), 3.71 (s, 2H), 3.91 (s, 3H), 5.03-5.08 (m, 2H), 5.39 (s, 1H), 5.88-5.95 (m, 1H), 6.43 (s, 1H), 6.65 (s, 1H), 7.84 (s, 1H), 10.40 (br s, 1H), 12.80 (br s, 1H). Mass spectrum (ES) MH+=357.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07652013B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-03ddf1633d094a53a303377997577b05 |
| Source note | uspto-grants-2010_01 |