HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808569Generated: November 1, 2026
Hydrochloric Acid → n-[1-{[4-(Aminomethyl)phenyl]methyl}-4-(methyloxy)-1h-indazol-3-yl]-5-chloro-2-thiophenesulfonamide formate salt
https://huagongshe.com/reaction/1808569
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 86661402 | HCID 86661402 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | n-[1-{[4-(Aminomethyl)phenyl]methyl}-4-(methyloxy)-1h-indazol-3-yl]-5-chloro-2-thiophenesulfonamide formate salt | HCID 66632574 | 83% |
Reaction Steps
To a solution of 1,1-dimethylethyl[(4-{[3-{[(5-chloro-2-thienyl)sulfonyl]amino}-4-(methyloxy)-1H-indazol-1-yl]methyl}phenyl)methyl]carbamate (for a preparation see Intermediate 29) (92 mg, 0.16 mmol) in dichloromethane (3 mL) was added dropwise hydrogen chloride (0.041 mL, 0.163 mmol). The resulting mixture was stirred at room temperature for 4 h, and then additional portion of hydrogen chloride (0.041 mL, 0.163 mmol) was added dropwise and the mixture was stirred at room temperature overnight. The solvents were then evaporated in a nitrogen blowdown unit. The residue was dissolved in 1:1 MeOH-DMSO (1 mL) and purified by Mass Directed AutoPrep (supelcosil ABZ+Plus column) eluting with solvents A/B (A: Water+0.1% Formic acid, B: MeCN:Water 95:5+0.05% Formic acid). The solvent was dried under a stream of nitrogen in the Radleys blowdown apparatus to give the title compound (69 mg, 83%). LCMS (System E) RT=2.10 min, ES+ve m/z 463/465 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08357716B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-9c618c316cca47888c6a80c6bd8ec472 |
|---|
| Source note | uspto-grants-2013_01 |
|---|