HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzaldehyde → HCID 25027763, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | 2-Chloro-4-fluorobenzaldehyde | HCID 145024 | — |
| Reactant | Nicotinamidine hydrochloride | HCID 202042 | — |
| Reactant | HCID 178479322 | HCID 178479322 | — |
| Product | HCID 25027763 | HCID 25027763 | 29% |
Reaction Steps
The method of Example 3 was used, wherein 3-pyridinecarboxamidine hydrochloride and 2-chloro-4-fluorobenzaldehyde were separately replaced by 2-amidinopyrazinium hydrochloride and 2-chlorobenzaldehyde to obtain a yellow solid of 0.21 g (yield 29%); 1H-NMR (400 MHz, CDCl3) δ 2.15-2.19 (2H, m, CH2); 2.45-2.85 (4H, s, CH2); 6.19 (1H, s, CH); 7.13-7.40 (4H, m, ArH); 8.27 (1H, s, ArH); 8.51 (H, m, ArH); 8.69 (H, m, ArH); 9.57 (1H, s, NH). MS (EI) 338.2 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08188091B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-713156a892804fceb0a1bb322194c3b6 |
| Source note | uspto-grants-2012_05 |