HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198122Generated: October 30, 2026
Methanesulfonyl chloride → HCID 86640801, compound
https://huagongshe.com/reaction/2198122
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 59278198 | HCID 59278198 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86640801 | HCID 86640801 | — |
Reaction Steps
A solution of 1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid [(S)-3-hydroxy-1-(2-methanesulfonyl-pyridin-4-yl)-propyl]-amide (0.10 g, 0.21 mmol) and N,N-diisopropylethylamine (167 μL, 0.957 mmol) in dichloromethane (20 mL) was cooled in an ice water-brine bath. After 5 minutes, methanesulfonyl chloride (25 μL, 0.32 mmol) was added and the cold bath was removed until the mixture became homogeneous. The mixture was again cooled in an ice bath. After 30 minutes, the mixture was quenched with saturated aqueous ammonium chloride (10 mL), washed with brine (10 mL), dried over magnesium sulfate and concentrated to afford methanesulfonic acid (S)-3-{[1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carbonyl]-amino}-3-(2-methanesulfonyl-pyridin-4-yl)-propyl ester which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338610B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-c03a5fdf14454c42bd3df7b973b1e41a |
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| Source note | uspto-grants-2012_12 |
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