HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803853Generated: November 1, 2026
Water → 3-chloromethyl-N-[5-(3,5-difluoro-benzyloxy)-1H-indazol-3-yl]-benzamide
https://huagongshe.com/reaction/1803853
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-(Chloromethyl)benzoyl chloride | HCID 2733324 | — |
| Reactant | 5-[(3,5-difluorobenzyl)oxy]-1H-indazol-3-amine | HCID 66997048 | — |
| Solvent | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Product | 3-chloromethyl-N-[5-(3,5-difluoro-benzyloxy)-1H-indazol-3-yl]-benzamide | HCID 46244831 | 56% |
Reaction Steps
5-(3,5-Difluoro-benzyloxy)-1H-indazol-3-ylamine (550 mg, 2 mmol) was dissolved in sym-collidine, cooled to 4° C. and treated with neat 3-chloromethyl-benzoyl chloride (0.34 mL, 2.4 mmol). After 1 hour the reaction mixture was added drop wise into iced water, with stirring and separation of a yellow oil occurred. Then, EtOAc (50 mL) and 2N HCl (25 mL) were added. The organic phase was separated, washed with aqueous NaHCO3 (50 mL), brine, dried over sodium sulfate and evaporated to dryness. After purification over silica gel (eluent: DCM:MeOH 95:5) 378 mg of title compound were obtained as a whitish solid in 56% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08354399B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-f75a9373fc1446e1beb6364fdd07b40d |
|---|
| Source note | uspto-grants-2013_01 |
|---|