HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483939Generated: October 29, 2026
Water → (S)-2-sulfamoylamino-6-((1-(3-methylbutanoyl)piperidin-3-yl)methoxy)benzonitrile
https://huagongshe.com/reaction/1483939
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Chlorosulfamic acid | HCID 24499 | — |
| Reactant | 2-Amino-6-(((3S)-1-(3-methyl-1-oxobutyl)-3-piperidinyl)methoxy)benzonitrile | HCID 86714278 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | (S)-2-sulfamoylamino-6-((1-(3-methylbutanoyl)piperidin-3-yl)methoxy)benzonitrile | HCID 86714277 | 87% |
Reaction Steps
To a stirred solution of (S)-2-amino-6-((1-(3-methylbutanoyl)piperidin-3-yl)methoxy)benzonitrile (example 5b, 54.55 g, 172.95 mmol) in DMA (110 mL) cooled to 0° C. in an ice bath was added sulfamoyl chloride (55 g, 476 mmol) in two portions (20 g and 35 g). The reaction mixture was stirred for 30 minutes at 0° C. under N2, then at room temperature for 4 hours. The reaction mixture was poured slowly into rapidly stirred cold water (2 L) to provide a milky solution. An additional 800 mL of water was added in several portions to precipitate the desired product (at this point the milky solution has become clear). The precipitate was collected by decantation of the water and was suspended in ethyl acetate (500 mL) then rapidly stirred until it became a fine white solid. The solid material was collected by vacuum filtration and dried under vacuum to give (S)-2-sulfamoylamino-6-((1-(3-methylbutanoyl)piperidin-3-yl)methoxy)benzonitrile as a white solid (59.25 g, 150.2 mmol) in 87% yield. MS 395 (MH+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09420814B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-6f6d20c60fd646169572205920566478 |
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| Source note | uspto-grants-2016_08 |
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