HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338759Generated: October 30, 2026
m-Tolyl isocyanate → HCID 71736173, compound
https://huagongshe.com/reaction/338759
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Tolyl isocyanate | HCID 69303 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86695872 | HCID 86695872 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71736173 | HCID 71736173 | 98.3% |
Reaction Steps
To a mixture of 4-(3,4-dihydro-2,7-naphthyridin-2(1H)-yl)-3-methylaniline trihydrochloride (24.7 mg, 0.071 mmol) and N,N-diisopropylethylamine (0.043 mL, 0.25 mmol) in 1.0 mL CH2Cl2 at rt was added meta-tolyl isocyanate (0.013 mL, 0.106 mmol) and the reaction stirred at rt for 1.5 hours. The reaction was quenched into a brine/aqueous Na2CO3 solution, then extracted with EtOAc. The EtOAc layer was washed with brine/aqueous Na2CO3 solution, dried with anhydrous Na2SO4, and evaporated to an oily solid. The oil was chromatographed eluting with CHCl3/EtOAc plus 0.5% MeOH to give the title compound as a faint yellow solid (26 mg, 97%). 1H NMR (Acetone-d6) δ: 8.35 (s, 1H), 8.32 (d, J=5.0 Hz, 1H), 7.97 (s, 1H), 7.93 (s, 1H), 7.29-7.40 (m, 4H), 7.08-7.17 (m, 3H), 6.80 (d, J=7.3 Hz, 1H), 4.07 (s, 2H), 3.15-3.20 (m, 2H), 2.97-3.03 (m, 2H), 2.30 (s, 3H), 2.29 (s, 3H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889870B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-ad47fb3ef53042dfabaa04f3057b42d5 |
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| Source note | uspto-grants-2014_11 |
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