HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633153Generated: October 26, 2026
Methyl 4-(bromomethyl)benzoate → HCID 178524403, compound
https://huagongshe.com/reaction/633153
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-(bromomethyl)benzoate | HCID 256687 | — |
| Reactant | HCID 178498016 | HCID 178498016 | — |
| Reactant | HCID 178498018 | HCID 178498018 | — |
| Reactant | HCID 178498019 | HCID 178498019 | — |
| Reactant | HCID 178527972 | HCID 178527972 | — |
| Product | HCID 178524403 | HCID 178524403 | — |
| Product | HCID 178524404 | HCID 178524404 | — |
Reaction Steps
500 mg of methyl 4-(bromomethyl)benzoate was reacted with 4H-1,2,4-triazole-3-thiol via Procedure Q. 542 mg of methyl 4-((4H-1,2,4-triazol-3-ylthio)methyl)benzoate was subsequently reacted via Procedure R to give an approximate 1:9 mixture of methyl 4-((4H-1,2,4-triazol-3-ylsulfinyl)methyl)benzoate and methyl 4-((4H-1,2,4-triazol-3-ylsulfonyl)methyl)benzoate. The mixture of 467 mg was hydrolyzed via Procedure M to give 4-((4H-1,2,4-triazol-3-ylsulfinyl)methyl)benzoic acid and 4-((4H-1,2,4-triazol-3-ylsulfonyl)methyl)benzoic acid. 107 mg of the mixture of 4-((4H-1,2,4-triazol-3-ylsulfinyl)methyl)benzoic acid and 4-((4H-1,2,4-triazol-3-ylsulfonyl)methyl)benzoic acid was coupled to 75 mg of 4-chloro-3-(pyridin-2-yl)aniline via Procedure G. The mixture was separated on reverse phase HPLC to give 4-((4H-1,2,4-triazol-3-ylsulfinyl)methyl)-N-(4-chloro-3-(pyridin-2-yl)phenyl)benzamide. MS (Q1) 438.1 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09321761B2 |
|---|
| Source dataset | uspto-grants-2016_04 |
|---|
| ORD ID | ord-64b667ef917d44afb933aa4ea802f400 |
|---|
| Source note | uspto-grants-2016_04 |
|---|