HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257759Generated: November 2, 2026
Water → 4-(6-Benzenesulfonyl-6H-1,2,3,5,6-pentaaza-as-indacen-1-yl)-1-methyl-cyclohexanol
https://huagongshe.com/reaction/1257759
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 4-(6-Benzenesulfonyl-6H-1,2,3,5,6-pentaaza-as-indacen-1-yl)-cyclohexanone | HCID 67343159 | — |
| Reactant | HCID 178419573 | HCID 178419573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(6-Benzenesulfonyl-6H-1,2,3,5,6-pentaaza-as-indacen-1-yl)-1-methyl-cyclohexanol | HCID 67344566 | — |
Reaction Steps
To a solution of 4-(6-Benzenesulfonyl-6H-1,2,3,5,6-pentaaza-as-indacen-1-yl)-cyclohexanone (400 mg, 1.01 mmol) in anhydrous tetrahydrofuran (20 mL) was added dropwise methylmagnesium bromine (3 M in diethyl ether, 2.3 mL, 7.07 mmol), followed by stirring at 0° C. for 30 minutes under nitrogen. The reaction was warmed to room temperature and stirred for another 90 minutes. The resulting mixture was poured into water and extracted with ethyl acetate. The organic solution was used for the next step. LCMS (Method K, ESI): RT=1.318 min and 1.359, m+H=411.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461328B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-3cc46c5071d847278e2a9172d0e880b2 |
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| Source note | uspto-grants-2013_06 |
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