HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycolaldehyde → HCID 178510393, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycolaldehyde | HCID 756 | — |
| Reactant | 4-Cyano-1h-imidazole-2-carboxylic acid (2-cyclohex-1-enyl-4-piperidin-4-yl-phenyl)-amide trifluoroacetic acid salt | HCID 178510383 | — |
| Product | HCID 178510393 | HCID 178510393 | — |
Reaction Steps
The title compound was prepared from 4-cyano-1H-imidazole-2-carboxylic acid (2-cyclohex-1-enyl-4-piperidin-4-yl-phenyl)-amide TFA salt (as prepared in Example 14, step (b)), and hydroxy-acetaldehyde according to the procedure in Example 21. 1H-NMR (400 MHz, CD3OD): δ 8.18 (d, 1H), 8.02 (s, 1H), 7.22 (dd, 1H), 7.14 (d, 2H), 5.82 (m, 1H), 3.94 (m, 2H), 3.74 (m, 2H), 3.30 (m, 2H), 3.18 (t, 2H), 2.92 (m, 1H), 2.30 (m, 4H), 2.20-1.98 (m, 4H), 1.96-1.74 (m, 4H). Mass spectrum (ESI, m/z): Calcd. for C24H29N5O2, 420.2 (M+H). found 420.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08933091B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-009431ca9c274a7cb13a554c01306f9c |
| Source note | uspto-grants-2015_01 |