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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047199Generated: October 31, 2026

Diisopropylethylamine → HCID 22258331, compound

https://huagongshe.com/reaction/1047199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPhenyl isoquinolin-5-ylcarbamateHCID 11380046—
ReactantHCID 22258334HCID 22258334—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 22258331HCID 2225833128.6%

Reaction Steps

1-Cyclopropylmethyl-6-fluoro-1,2,3,4-tetrahydro-naphthalen-2-ylamine hydrochloride (127 mg, 0.49 mmol), isoquinolin-5-yl-carbamic acid phenyl ester (150 mg, 0.49 mmol), and diisopropylethylamine (193 mg, 1.47 mmol) were combined and stirred at ambient temperature in DMSO (3 mL) overnight. 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-cyclopropylmethyl-6-fluoro-1,2,3,4-tetrahydro-naphthalen-2-yl)-3-isoquinolin-5-yl-urea 71 (68 mg, 0.14 mmol). MS (MH+) 390; 1H NMR (CD3OD) δ 0.08-0.87 (m, 2H), 1.60-1.65 (m, 2H), 2.03 (m, 1H), 2.97 (m, 2H), 3.14 (m, 1H), 4.36 (m, 1H), 6.87 (m, 2H), 7.27 (m, 1H), 7.93 (t, 1H, J=2.6 Hz), 8.14 (d, 1H, J=2.7 Hz), 8.32 (d, 1H, J=2.2 Hz), 8.47 (d, 1H, J=2.6 Hz), 8.53 (d, 1H, J=2.2 Hz), 9.63 (s, 1H). HPLC Rt=3.63 min (10-90% water:acetonitrile gradient, 100% pure).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569505B2
Source datasetuspto-grants-2013_10
ORD IDord-276c52835e6b459b979bd2ecb8d37162
Source noteuspto-grants-2013_10