HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251695Generated: October 30, 2026
Hydroxylamine → 6-(4-((5-fluoro-2-oxoindolin-3-ylidene)methyl)benzamido)-N-hydroxyhexanamide
https://huagongshe.com/reaction/251695
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 6-(4-((5-Fluoro-2-oxoindolin-3-ylidene)methyl)benzamido)hexanoic acid | HCID 69032748 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 6-(4-((5-fluoro-2-oxoindolin-3-ylidene)methyl)benzamido)-N-hydroxyhexanamide | HCID 76603895 | 46% |
Reaction Steps
6-(4-((5-fluoro-2-oxoindolin-3-ylidene)methyl)benzamido)hexanoic acid (396 mg, 1 mmol), triethylamine (151 mg, 1.5 mmol) and 20 ml of DMF were stirred at 0° C. while ethyl chloroformate (163 mg, 1.5 mmol) was added. The mixture was stirred at 0° C. for 2 hours, and then 50% aqueous solution of hydroxylamine (1.32 g, 20 mmol) was added. The mixture was stirred for 3 hours at room temperature, and then diluted with 1000 mL of brine. The solids were collected by vacuum filtration, washed with water and dried under vacuum to give the title compound (189 mg, 46%) as a brown solid. LC-MS (m/z) 412 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863315B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-9233d2e9b3ca4d0ebd43806534b8c48c |
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| Source note | uspto-grants-2011_01 |
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