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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849577Generated: November 1, 2026

Tricyclo(3.3.1.1'3,7)dec-1-ylmethanol → HCID 91809366, compound

https://huagongshe.com/reaction/1849577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTricyclo(3.3.1.1'3,7)dec-1-ylmethanolHCID 64556—
Reactant[(1S)-endo]-(-)-BorneolHCID 1201518—
Reactant5-chloro-2,4-difluoro-N-(methylsulfonyl)benzamideHCID 58042417—
Reactant5-chloro-N-(N,N-dimethylsulfamoyl)-2,4-difluorobenzamideHCID 86702836—
ProductHCID 91809366HCID 91809366—

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 [(1S)-endo]-(−)-borneol, the title compound was obtained as a colorless solid (0.17 g, 34%): 1H NMR (300 MHz, CDCl3) δ 8.64 (s, 1H), 8.20-8.00 (m, 1H), 6.67-6.43 (m, 1H), 4.47-4.25 (m, 1H), 3.03 (s, 6H), 2.55-2.20 (m, 2H), 1.92-1.69 (m, 2H), 1.51-1.19 (m, 2H), 1.19-0.74 (m, 10H); MS (ES−) m/z 431.2 (M−1), 433.2 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952169B2
Source datasetuspto-grants-2015_02
ORD IDord-f9c58368de51485db34957a00f93c3b2
Source noteuspto-grants-2015_02