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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920698Generated: October 29, 2026

(S)-2-(Piperidin-2-yl)ethanamine → HCID 54713622, compound

https://huagongshe.com/reaction/920698

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-(Piperidin-2-yl)ethanamineHCID 667728—
ReactantHCID 66594467HCID 66594467—
ProductHCID 54713622HCID 54713622155.6%

Reaction Steps

In a manner similar to that described in example Z-35, from {2-[(2S)-2-piperidinyl]ethyl}amine (28 mg, 0.218 mmol) and 16a (30 mg, 0.0638 mmol) was prepared (4aS,14aS)-N-[(2,4-difluorophenyl)methyl]8,10-dioxo-9-[(phenylmethyl)oxy]-2,3,4,4a,5,6,8,10,14,14a-decahydro-1H-pyrido[1,2-c]pyrido[1′,2′:4,5]pyrazino[1,2-a]pyrimidine-11-carboxamide (20 mg, 82%). This material was deprotected in a second step similar to that described in example Z-37 to give the title compound as a white solid (26 mg, quantitative). 1H NMR (CDCl3) δ 12.44 (br s, 1H), 10.48 (s, 1H), 8.26 (s, 1H), 7.35 (m, 1H), 6.80 (m, 2H), 4.68-4.57 (m, 2H), 4.38 (m, 1H), 4.20 (m, 1H), 3.93 (s, 1H), 3.63-3.39 (m, 2H), 2.91 (m, 2H), 2.29 (br s, 1H), 2.02 (m, 1H), 1.69-1.45 (m, 4H), 1.80-1.24 (m, 2H), 1.12 (br s, 1H); ES+MS: 459 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273065B2
Source datasetuspto-grants-2016_03
ORD IDord-f26489e478884e63945874bb44e90483
Source noteuspto-grants-2016_03