Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849652Generated: October 30, 2026

Tricyclo(3.3.1.1'3,7)dec-1-ylmethanol → HCID 86703515, compound

https://huagongshe.com/reaction/1849652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTricyclo(3.3.1.1'3,7)dec-1-ylmethanolHCID 64556—
Reactant(Spiro(2.5)octan-6-yl)methanolHCID 53487089—
Reactant5-chloro-2,4-difluoro-N-(methylsulfonyl)benzamideHCID 58042417—
ReactantHCID 86703514HCID 86703514—
ProductHCID 86703515HCID 86703515—

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-(cyclopropylsulfonyl)-2,4-difluorobenzamide and to replace adamantan-1-ylmethanol with spiro[2.5]octan-6-ylmethanol, the title compound was obtained as a colorless solid (0.165 g, 28%): 1H NMR (300 MHz, CDCl3) δ8.72-8.59 (m, 1H), 8.16-8.07 (m, 1H), 6.76-6.65 (m, 1H), 3.97-3.86 (m, 2H), 3.17-3.05 (m, 1H), 2.03-1.72 (m, 5H), 1.51-1.42 (m, 2H), 1.36-1.11 (m, 4H), 1.00-0.90 (m, 2H), 0.38-0.14 (m, 4H); MS (ES+) m/z 416.2, 418.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952169B2
Source datasetuspto-grants-2015_02
ORD IDord-456b60b4cfdb42ef8a08ef5c25a71224
Source noteuspto-grants-2015_02