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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268736Generated: October 26, 2026

7-Methanesulfonyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine → N-[4-(3-Piperidin-1-yl propoxy)benzoyl]-7-methylsulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine Hydrochloride

https://huagongshe.com/reaction/268736

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Methanesulfonyl-2,3,4,5-tetrahydro-1H-benzo[d]azepineHCID 11736266—
Reactant4-(3-Piperidin-1-ylpropoxy)benzoyl chloride hydrochlorideHCID 21852062—
ProductN-[4-(3-Piperidin-1-yl propoxy)benzoyl]-7-methylsulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine HydrochlorideHCID 68963945—

Reaction Steps

The title compound was prepared from 4-(3-piperidin-1-ylpropoxy)benzoyl chloride hydrochloride (D3) (0.20 g) and 7-methanesulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine (WO00/21951) (0.17 g) using the procedure described for Example 1 and isolated as a white solid (0.24 g). MS electrospray (+ion) 471 (MH+). 1H NMR δ (DMSO-d6): 9.83 (1H, s), 7.71 (2H, m), 7.44 (1H, s), 7.35 (2H, d, J=8.5 Hz ), 7.01 (2H, d, J=8.6 Hz), 4.11 (2H, t, J=5.9 Hz), 3.71-3.45 (6H, m), 3.18 (6H, m), 3.05 (3H, s) 2.87 (2H, m), 2.20 (2H, m), 1.83-1.37 (6H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446103B2
Source datasetuspto-grants-2008_11
ORD IDord-1874cb0957754563a2997cd3330d3af1
Source noteuspto-grants-2008_11