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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078907Generated: October 26, 2026

N,N-Dimethylpiperidin-4-amine → N-(2,4-dichlorophenyl)-9-(4-(dimethylamino)piperidine-1-carbonyl)-N-methyl-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-2-carboxamide

https://huagongshe.com/reaction/2078907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Dimethylpiperidin-4-amineHCID 417391—
Reactant2-[(2,4-Dichloro-phenyl)-methyl-carbamoyl]-4,5-dihydro-6-oxa-1-thia-benzo[e]azulene-9-carboxylic acidHCID 66868922—
ProductN-(2,4-dichlorophenyl)-9-(4-(dimethylamino)piperidine-1-carbonyl)-N-methyl-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-2-carboxamideHCID 57900140—

Reaction Steps

2-[(2,4-Dichloro-phenyl)-methyl-carbamoyl]-4,5-dihydro-6-oxa-1-thia-benzo[e]azulene-9-carboxylic acid and 4-(dimethylamino)piperidine were reacted by General Procedure B to give 247. NMR: (CDCl3): 1.45-1.62 (2H, br m), 1.88-2.01 (2H, br, m), 2.39 (6H, s, Me), 2.50-2.61 (1H, br m), 2.82-3.10 (2H, br m), 3.07-3.09 (2H, m), 3.38 (3H, s, Me), 3.80-4.01 (1H, br m), 4.26-4.29 (2H, m), 4.58-4.79 (1H, br m), 6.85 (1H, s, Ar), 7.02 (1H, d, J 8.3, Ar), 7.25 (1H, dd, J 8.2 and 2.0, Ar), 7.28-7.32 (1H, m, Ar), 7.37-7.39 (1H, m, Ar), 7.55 (1H, s, Ar) and 7.60 (1H, s, Ar). MS: (ESI+) MH+=558.14

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928248B2
Source datasetuspto-grants-2011_04
ORD IDord-4b6a7ab46dd349d3ac8ac2fb45fe957a
Source noteuspto-grants-2011_04