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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244128Generated: November 1, 2026

Sodium Bicarbonate → HCID 11317113, compound

https://huagongshe.com/reaction/2244128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant1-Benzyl-6-fluoro-1,2,3,4-tetrahydro-naphthalen-2-ylamine hydrochlorideHCID 22258317—
ReactantPhenyl (1-chloroisoquinolin-5-yl)carbamateHCID 71382112—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 11317113HCID 1131711328%

Reaction Steps

(1-Chloro-isoquinolin-5-yl)-carbamic acid phenyl ester (150 mgs, 0.5 mmol), 1-Benzyl-6-fluoro-1,2,3,4-tetrahydro-naphthalen-2-ylamine hydrochloride (146 mgs, 0.5 mmol), and sodium bicarbonate (42 mgs, 0.5 mmol) were combined and stirred for one hour in DMSO (4 ml) at ambient temperature. The product was purified by directly injecting the crude reaction onto a reverse phase prep-HPLC (10-90% water:acetonitrile gradient). The appropriate fractions were lyophilized to yield 1-(1-Benzyl-6-fluoro-1,2,3,4-tetrahydro-naphthalen-2-yl)-3-(1-chloro-isoquinolin-5-yl)-urea (64 mgs, 28%) MS (MH+) 459; 1H NMR (CD3OD) δ 1.93-2.06 (m, 1H), 2.09-2.13 (m, 1H), 2.91-3.07 (m, 4H), 3.40-3.42 (m, 1H), 4.07-4.10 (s, 1H), 6.69-6.78 (m, 1H), 6.80-6.89 (m, 2H), 7.12-7.26 (m, 5H), 7.72 (t, 1H, J=8.2 Hz), 7.83 (d, 1H, J=6.1 Hz), 8.19 (d, 1H, J=8.6 Hz), 8.17-8.24 (m, 2H). HPLC Rt=4.04 min (50-90% water:acetonitrile gradient, 100% pure).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678812B2
Source datasetuspto-grants-2010_03
ORD IDord-ddc2b8eb14704712a7f6a5a0461b1e92
Source noteuspto-grants-2010_03