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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036253Generated: November 1, 2026

L-Lactic Acid → HCID 178462374, compound

https://huagongshe.com/reaction/2036253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Lactic AcidHCID 107689—
ReactantHCID 178512153HCID 178512153—
SolventEthanolHCID 702—
ProductLactic AcidHCID 612—
ProductHCID 178462374HCID 178462374158.2%

Reaction Steps

To a solution of 2,4-diamino-5-chloro-N—(N-{4-[4-(2,3-dihydroxypropoxy)naphthalen-1-yl]butyl}carbamimidoyl)benzamide (24, 28 mg, 0.06 mmole) in EtOH (10 mL) was added L-(+)-lactic acid (5.20 mg, 0.06 mmole) at room temperature and the reaction mixture was stirred for 15 min. The solution was concentrated and the residue was azeotroped with MeOH. The residue was dissolved in H2O (3 mL) and lyophilized to afford lactic acid salt 26 (28 mg, 84%) as a yellow solid: mp 115-118° C.; 1H NMR (300 MHz, CD3OD) δ 8.32 (d, J=8.4 Hz, 1H), 8.01 (d, J=8.4 Hz, 1H), 7.53-7.40 (m, 2H), 7.24 (d, J=7.8 Hz, 1H), 6.83 (d, J=7.8 Hz, 1H), 4.21-4.10 (m, 3H), 4.01-3.94 (m, 1H), 3.82-3.73 (m, 2H), 3.35-3.33 (m, 2H), 3.08 (t, J=7.0, Hz, 1H), 1.89-1.77 (m, 4H), 1.31 (d, J=7.0 Hz, 3H); ESI-MS m/z 524 [C23H28ClN7O4+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575176B2
Source datasetuspto-grants-2013_11
ORD IDord-5be636df4dd8416c8ea605776ef91c2f
Source noteuspto-grants-2013_11