HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117129Generated: October 29, 2026
N-bromobutanimide → 5-(Bromomethyl)-4-chloropyrrolo[2,1-f][1,2,4]triazine
https://huagongshe.com/reaction/2117129
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Chloro-5-methylpyrrolo(2,1-f)(1,2,4)triazine | HCID 21874227 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 5-(Bromomethyl)-4-chloropyrrolo[2,1-f][1,2,4]triazine | HCID 21874386 | 92% |
Reaction Steps
A mixture of 4-chloro-5-methyl-pyrrolo[2,1-f][1,2,4]triazine (2.0 g, 11.93 mmol, WO 03/042172) and AKIN (195 mg, 1.19 mmol) in CCl4 (80 mL) under N2 was heated to 100° C. for 5 min, NBS (2.55 g, 14.3 mmol) was added. The reaction mixture was stirred for 10 min, then cooled to rt, filtered. The CCl4 layer was washed with dilute NaHCO3 aqueous solution, dried (MgSO4), filtered and concentrated to give the desired product (2.70 g, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07439246B2 |
|---|
| Source dataset | uspto-grants-2008_10 |
|---|
| ORD ID | ord-bbbe905d422f4b62bebbfbf6a0bb124f |
|---|
| Source note | uspto-grants-2008_10 |
|---|