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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849540Generated: November 1, 2026

Tricyclo(3.3.1.1'3,7)dec-1-ylmethanol → HCID 86702884, compound

https://huagongshe.com/reaction/1849540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTricyclo(3.3.1.1'3,7)dec-1-ylmethanolHCID 64556—
Reactant(3-Fluorotricyclo[3.3.1.1~3,7~]decan-1-yl)methanolHCID 21634598—
Reactant5-chloro-2,4-difluoro-N-(methylsulfonyl)benzamideHCID 58042417—
Reactant5-chloro-N-(N,N-dimethylsulfamoyl)-2,4-difluorobenzamideHCID 86702836—
ProductHCID 86702884HCID 86702884—

Reaction Steps

Following the procedure as described in Example 8 and making variations as required to replace 5-chloro-2,4-difluoro-N-(methylsulfonyl)benzamide with 5-chloro-N— (N,N-dimethylsulfamoyl)-2,4-difluorobenzamide and adamantan-1-ylmethanol with 3-fluoroadamantan-1-yl methanol, the title compound was obtained as a colorless solid (0.16 g, 35%): 1H NMR (300 MHz, DMSO-d6) δ 11.77 (s, 1H), 7.73 (d, J=7.4 Hz, 1H), 7.23 (d, J=12.3 Hz, 1H), 3.84 (s, 2H), 2.87 (s, 6H), 2.30 (br s, 2H), 1.87-1.76 (m, 6H), 1.61-1.52 (m, 6H); MS (ES−) m/z 461.1, 463.1 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952169B2
Source datasetuspto-grants-2015_02
ORD IDord-ea3e1b7b5eb0448eb5752b69e8081c8a
Source noteuspto-grants-2015_02