HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472211Generated: October 30, 2026
Diisopropylethylamine → HCID 57703904, compound
https://huagongshe.com/reaction/1472211
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3,5-Difluorobenzenesulfonyl chloride | HCID 2774058 | — |
| Reactant | HCID 67009100 | HCID 67009100 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57703904 | HCID 57703904 | — |
Reaction Steps
3,5-difluoro-benzenesulfonyl chloride (1 eq., 3.9 g, 18.4 mmol) was added portion-wise to a stirred solution of 6,6-dimethyl-3-[4-(4-methyl-piperazin-1-yl)-2-nitro-benzoylamino]-5,6-dihydro-4H-pyrrolo[3,4-c]pyrazole-2-carboxylic acid ethyl ester dihydrochloride (10 g, 18.4 mmol) and N,N-diisopropylethylamine (6 eq, 19.3 mL, 110.4 mmol) in dry dichloromethane (100 mL) at room temperature. Stirring was continued for about 4 hours. The reaction mixture was diluted with dichloromethane (100 mL) then washed with saturated sodium hydrogen carbonate (150 mL), dried over sodium sulphate, evaporated to dryness and purified by flesh chromatography on silica gel using acetone as the eluant. The title compound was obtained as yellow solid (9 g, 65% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012487B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-308e10cf5a01449788f2519a3f88a165 |
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| Source note | uspto-grants-2015_04 |
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