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
Participants
| Role | Name | HCID | Charge |
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| Reactant | (S)-2-(Piperidin-2-yl)ethanamine | HCID 667728 | — |
| Reactant | HCID 66594467 | HCID 66594467 | — |
| Product | HCID 54713622 | HCID 54713622 | 155.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273065B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-f26489e478884e63945874bb44e90483 |
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| Source note | uspto-grants-2016_03 |
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