HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472258Generated: October 30, 2026
4-(4-Bromophenyl)morpholine → HCID 49838138, compound
https://huagongshe.com/reaction/472258
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(4-Bromophenyl)morpholine | HCID 11622851 | — |
| Reactant | 8-(4-Methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine | HCID 57502376 | — |
| Product | HCID 49838138 | HCID 49838138 | — |
| Product | HCID 57502379 | HCID 57502379 | — |
Reaction Steps
[8-(4-Methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-(4-morpholin-4-yl-phenyl)-amine and [8-(4-methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-phenyl-amine were prepared from 8-(4-methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine (100.0 mg, 0.3468 mmol) and 4-(4-bromo-phenyl)-morpholine (100.0 mg, 0.4130 mmol) in a manner analogous to Example 2d. [8-(4-Methanesulfonyl-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl]-(4-morpholin-4-yl-phenyl)-amine was isolated as a pale yellow solid (0.063 g, 40%). MP=244-246° C. 1H NMR (400 MHz, CDCl3, δ, ppm): 8.49-8.45 (m, 1H), 8.25-8.20 (m, 2H), 8.11-8.06 (m, 2H), 7.63 (dd, J=7.4, 0.9 Hz, 1H), 7.53-7.48 (m, 2H), 6.99 (t, J=7.0 Hz, 1H), 6.97-6.93 (m, 2H), 6.73 (s, 1H), 3.90-3.86 (m 4H), 3.14-3.09 (m, 7H). MS=450 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08633173B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-e276c8f419fd43f886dcbaa4e0bde783 |
|---|
| Source note | uspto-grants-2014_01 |
|---|