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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338755Generated: October 30, 2026

m-Tolyl isocyanate → HCID 71738047, compound

https://huagongshe.com/reaction/338755

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Tolyl isocyanateHCID 69303—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86695868HCID 86695868—
SolventDichloromethaneHCID 6344—
ProductHCID 71738047HCID 7173804788%

Reaction Steps

To a mixture of 4-(3,4-dihydro-2,7-naphthyridin-2(1H)-yl)aniline dihydrochloride (75.0 mg, 0.251 mmol) and N,N-diisopropylethylamine (0.109 mL, 0.63 mmol) in 3.0 mL CH2Cl2 at rt was added meta-tolyl isocyanate (0.047 mL, 0.377 mmol) and the reaction stirred at rt for 2 hours. The reaction was quenched with 1.0 mL MeOH, stirred for 15 min and then evaporated. The sample was partitioned between EtOAc and H2O/brine mixture, the EtOAc layer washed with aqueous Na2CO3 solution, brine, dried with anhydrous Na2SO4, and evaporated to a tan solid. The solid was chromatographed eluting with CH2Cl2, EtOAc, then 3% MeOH/EtOAc to give the title compound as a white solid (79 mg, 88%). 1H NMR (DMSO-d6) δ: 8.45 (s, 1H), 8.42 (s, 1H), 8.37 (s, 1H), 8.31 (d, J=5.0 Hz, 1H), 7.29-7.35 (m, 2H), 7.28 (s, 1H), 7.16-7.23 (m, 2H), 7.10-7.16 (m, 1H), 6.96-7.02 (m, 2H), 6.76 (d, J=7.0 Hz, 1H), 4.33 (s, 2H), 3.47 (t, J=5.9 Hz, 2H), 2.91 (t, J=5.7 Hz, 2H), 2.27 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889870B2
Source datasetuspto-grants-2014_11
ORD IDord-672bfc0ab9c84b9c93b4758929fc7630
Source noteuspto-grants-2014_11