HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490560Generated: October 31, 2026
Hydrochloric Acid → 5-amino-1-(4-chloro-benzyl)-1,2-dihydro-indazol-3-one
https://huagongshe.com/reaction/490560
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 68833180 | HCID 68833180 | — |
| Product | 5-amino-1-(4-chloro-benzyl)-1,2-dihydro-indazol-3-one | HCID 10564210 | 76.4% |
Reaction Steps
To 1-(4-chloro-benzyl)-5-nitro-1,2-dihydro-indazol-3-one (0.45 g) was added HCl (37% aq.) solution (5 mL) followed by SnCl2.dihydrate (1.9 g). The mixture was heated to 85° C. for one hour. The reaction was then neutralized with sodium bicarbonate solution, filtered, and the filtrate extracted with EtOAc. The combined organic phases were washed with brine, dried over sodium sulfate, filtered and reduced in vacuo. Flash column chromatography of the residue over silica gel eluting with methylene chloride/methanol afforded the desired 5-amino-1-(4-chloro-benzyl)-1,2-dihydro-indazol-3-one (0.31 g) as a dark brown solid. MS (ESI+): 274.4 [M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528158B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-bae5617fcf07438d8df71446bcf95b0b |
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| Source note | uspto-grants-2009_05 |
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