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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430516Generated: October 28, 2026

1,3-Difluoro-5-isocyanatobenzene → HCID 86713661, compound

https://huagongshe.com/reaction/1430516

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Difluoro-5-isocyanatobenzeneHCID 2779282—
ReactantHCID 89611458HCID 89611458—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86713661HCID 8671366169.3%

Reaction Steps

A solution of Example A7 (0.12 g, 0.266 mmol) in dioxane (5 mL) was treated with 3,5-difluorophenyl isocyanate (0.038 mL, 0.320 mmol) and stirred at RT overnight. Additional 3,5-difluorophenyl isocyanate (0.038 mL, 0.320 mmol) was added and the mixture stirred for 4 h. The resulting precipitate was collected via filtration and dried to yield 1-(5-(7-((4-methoxybenzyl)(methyl)amino)-1-ethyl-2-oxo-1,2,4a,8a-tetrahydro-1,6-naphthyridin-3-yl)-2,4-difluorophenyl)-3-(3,5-difluorophenyl)urea (112 mg, 69% yield). 1H NMR (400 MHz, DMSO-d6): δ 9.38 (s, 1H), 8.67 (s, 1H), 8.52 (s, 1H), 8.05 (t, 1H), 7.86 (s, 1H), 7.38 (t, 1H), 7.19-7.14 (m, 4H), 6.86 (d, 2H), 6.80-6.77 (m, 1H), 6.32 (s, 1H), 4.85 (s, 2H), 4.19 (q, 2H), 3.70 (s, 3H), 3.12 (s, 3H), 1.13 (t, 3H); MS (ESI) m/z: 606.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940756B2
Source datasetuspto-grants-2015_01
ORD IDord-9a879b6efabe42beb5f760045bd506ee
Source noteuspto-grants-2015_01