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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191124Generated: October 31, 2026

4-Piperidin-1-ylmethyl-benzylamine → HCID 86624169, compound

https://huagongshe.com/reaction/1191124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Piperidin-1-ylmethyl-benzylamineHCID 5200292—
Reactant7-Chloro-3-(2,2,2-trifluoroacetyl)-6-trifluoromethylsulfonyloxy-2,3,4,5-tetrahydro-1H-benzo[d]azepineHCID 57447747—
ProductHCID 86624169HCID 8662416972.5%

Reaction Steps

Use a method similar to the General Procedure)-2 to couple 7-chloro-3-(2,2,2-trifluoroacetyl)-6-trifluoromethansulfonyloxy-2,3,4,5-tetrahydro-1H-benzo[d]azepine (300 mg, 0.69 mmol) and 4-(piperidin-1-ylmethyl)-benzylamine (174 mg, 0.84 mmol). Purify by chromatography on silica gel (150 g) eluting with a gradient of DCM to 4:1 DCM/(chloroform:methanol:concentrated NH4OH 80:18:2) to obtain 7-chloro-6-[4-(piperidin-1-ylmethyl)-benzylamino]-3-(2,2,2-trifluoroacetyl)-2,3,4,5-tetrahydro-1H-benzo[d]azepine as an oil (240 mg, 71%). MS (ES+) m/z: 480 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680091B2
Source datasetuspto-grants-2014_03
ORD IDord-0067b3e6680b4381944ffc97f366f915
Source noteuspto-grants-2014_03