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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862676Generated: October 30, 2026

Ethyl (3S)-3-amino-3-(pyridin-3-yl)propanoate--hydrogen chloride (1/2) → (S)-3-[2-(1-Oxo-7-piperazin-1-yl-3,4-dihydro-1H-isoquinolin-2-yl)-acetylamino]-3-pyridin-3-yl-propionic acid

https://huagongshe.com/reaction/862676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (3S)-3-amino-3-(pyridin-3-yl)propanoate--hydrogen chloride (1/2)HCID 44891224—
ReactantN-{[7-(Piperazin-1-yl)-3,4-dihydro-1(1H)-isoquinolinone-2-yl]acetyl}-2(R)-(phenylsulfonylamino)-beta-alanineHCID 86752094—
Product(S)-3-[2-(1-Oxo-7-piperazin-1-yl-3,4-dihydro-1H-isoquinolin-2-yl)-acetylamino]-3-pyridin-3-yl-propionic acidHCID 10789118—

Reaction Steps

Following the procedure described for 1-7, but substituting 2(R)-(phenylsulfonylamino)-β-alanine for ethyl 3-amino-3(S)-(3-pyridyl)propionate dihydrochloride, the title compound was prepared. 1H NMR (CD3OD): δ 1.50 (9H, s), 3.00 (2H, m), 3.18 (2H, m), 3.3-3.7 (10H, m), 4.09 (1H, dd), 4.23 (2H, m), 7.2 (2H, m), 7.5-7.6 (4H, m), 7.85 (2H, m), 8.22 (1H, m). ##STR43## N-{[7-(Piperazin-1-yl)-3,4-dihydro-1(1H) -isoquinolinone-2-yl]acetyl}-2(R)-(phenylsulfonylamino)-β-alanine (1-22)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719162
Source datasetuspto-grants-1998_02
ORD IDord-f4f8204ff8eb43518db97658b1ca0058
Source noteuspto-grants-1998_02