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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880958Generated: November 2, 2026

p-Toluenesulfonic acid monohydrate → HCID 57955658, compound

https://huagongshe.com/reaction/1880958

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantMethyl 4-amino-2-fluoro-5-methoxybenzoateHCID 57955533—
ReactantHCID 57955604HCID 57955604—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57955658HCID 5795565840%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of (R)-2-chloro-9-cyclopentyl-7-fluoro-5-methyl-7-vinyl-8,9-dihydro-5H-pyrimido[4,5-b][1,4]diazepin-6(7H)-one (1.0 g, 3.086 mmol), and methyl 4-amino-2-fluoro-5-methoxybenzoate (3.07 g, 15.43 mmol) was dissolved in dioxane (20 ml), and p-toluenesulfonic acid, monohydrate (2.99 g, 15.74 mmol) was added. The mixture was stirred at 95° C. for 24-48 h. The final compound was purified by reverse phase HPLC to give 400 mg product as white solid (40%). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.48-1.82 (m, 4 H) 1.93-1.98 (m, 4 H) 3.29 (s, 3 H) 3.51 (br. s., 2 H) 3.61 (m, 3 H), 3.86 (m, 3 H) 3.94 (s, 3 H) 4.88 (t, J=8.08 Hz, 1 H) 5.30-5.47 (m, 2 H) 6.01 (ddd, J=17.43, 12.63, 10.86 Hz, 1 H) 7.41-7.57 (m, 1 H) 7.82 (s, 1 H) 8.12 (s, 1 H) 8.31 (d, J=8.08 Hz, 1 H). [M+H] calc'd for C24H27F2N5O4, 488; found 488.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318727B2
Source datasetuspto-grants-2012_11
ORD IDord-ffb5a4e0805a4c4f9106f0700b34061d
Source noteuspto-grants-2012_11