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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246707Generated: November 2, 2026

1-Tert-butyl-4-isocyanatobenzene → N-(4-tert-butylphenyl)-3-(3-chloro-2-pyridinyl)-3,8-diazabicyclo[3.2.1]octane-8-carboxamide

https://huagongshe.com/reaction/1246707

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Tert-butyl-4-isocyanatobenzeneHCID 2735695—
Reactant3-(3-Chloropyridin-2-yl)-3,8-diazabicyclo[3.2.1]octaneHCID 21904768—
SolventDichloromethaneHCID 6344—
ProductN-(4-tert-butylphenyl)-3-(3-chloro-2-pyridinyl)-3,8-diazabicyclo[3.2.1]octane-8-carboxamideHCID 11463692—

Reaction Steps

3-(3-Chloro-2-pyridinyl)-3,8-diazabicyclo[3.2.1]octane (129 mg, 577 μmol) in dry dichloromethane (5 mL) was treated with 1-tert-butyl4-isocyanatobenzene (101 mg, 577 μmol) and allowed to stir overnight at room temperature. The mixture was concentrated under reduced pressure and the residue was purified by chromatography on silica gel (3:1, hexanes:ethyl acetate) to provide the title compound. MS (DCI/NH3) m/z: 399 (M+H)+; 1H NMR (CDCl3) δ 1.30 (s, 9H), 2.01 (m, 2H), 2.17 (m, 2H), 3.25 (d, 2H), 3.64 (dd, 2H), 4.38 (dd, 2H), 6.32 (s, 1H), 6.86 (dd, 1H), 7.32 (s, 4H), 7.59 (dd, 1H), 8.17 (dd, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129235B2
Source datasetuspto-grants-2006_10
ORD IDord-3ed89a53f9d44dc79597729fdbb6a2b1
Source noteuspto-grants-2006_10