HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chlorobenzyl alcohol → 2-(3-Chlorobenzyloxy)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chlorobenzyl alcohol | HCID 70117 | — |
| Reactant | 2-Methylthio-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)pyrimidine | HCID 69198971 | — |
| Product | 2-(3-Chlorobenzyloxy)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)pyrimidine | HCID 59753942 | — |
Reaction Steps
2-Methylthio-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)pyrimidine from Reference Example 3 was reacted with 3-chlorobenzyl alcohol according to the procedure described in Example 59 to afford 2-(3-chlorobenzyloxy)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)pyrimidine (HRf): HPLC/MS: m/e=475 (M++1); Rt=4.92 min; 1H-NMR 400 MHz (CDCl3): δ 5.58 (s, 2H), 7.15 (d, J=9 Hz, 1H), 7.25-7.38 (m, 7H), 7.40-7.50 (m, 2H), 7.58 (s, 1H), 8.48 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07405221B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-d760416164644154bec5dd7532f979a7 |
| Source note | uspto-grants-2008_07 |