HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167984Generated: October 26, 2026
Diisopropylamine → 4-(1-(2,2-Difluoroethyl)piperidin-4-ylamino)-3-nitrobenzenesulfonamide
https://huagongshe.com/reaction/2167984
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 1,1-Difluoro-2-iodoethane | HCID 3833565 | — |
| Reactant | HCID 67170227 | HCID 67170227 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(1-(2,2-Difluoroethyl)piperidin-4-ylamino)-3-nitrobenzenesulfonamide | HCID 48934007 | — |
Reaction Steps
3-nitro-4-(piperidin-4-ylamino)benzenesulfonamide hydrochloride (0.100 g), 1,1-difluoro-2-iodoethane (0.063 mL) and diisopropylamine (0.156 mL) were stirred together in N,N-dimethylformamide (3 ml) and heated to 85° C. The reaction was diluted with dichloromethane (50 mL) and washed with water (50 mL), brine (50 mL), dried over magnesium sulfate, filtered, and concentrated. The residue was loaded onto silica gel (GraceResolve 12 g) and eluted using a gradient of 0.5% methanol/dichloromethane to 3% methanol/dichloromethane over 30 minutes to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045475B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-0c9557057d7a4e4f88c82d65a3d50788 |
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| Source note | uspto-grants-2015_06 |
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