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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014470Generated: October 31, 2026

Naphthalene → HCID 178486468, compound

https://huagongshe.com/reaction/1014470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNaphthaleneHCID 931—
ReactantWaterHCID 962—
ReactantSodiumHCID 5360545—
ReactantHCID 59442045HCID 59442045—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178486468HCID 17848646833%

Reaction Steps

To a degassed solution of naphthalene (14 g, 109 mmol) in THF (300 mL) were added sodium cubes (2.6 g, 108 mmol). The cubes were crushed, and then stirred for 4 h. A total of 60 mL of the resulting deep green solution was added dropwise to a −78° C. solution of 2-fluoro-6-({2-({5-(methyloxy)-1-[(4-methylphenyl)sulfonyl]-2,3-dihydro-1H-indol-6-yl}amino)-7-[(4-methylphenyl)sulfonyl]-7H-pyrrolo[2,3-d]pyrimidin-4-yl}amino)benzamide (3.7 g, 4.99 mmol) in THF (100 mL). Water (5 mL) was then added, the resulting mixture was allowed to warm to rt, and filtered. The filtrate was concentrated onto Celite and purified by silica gel chromatography using 1-10% MeOH (containing 0.2% NH3)/CH2Cl2 to obtain 2-fluoro-6-[(2-{[5-(methyloxy)-2,3-dihydro-1H-indol-6-yl]amino}-1H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]benzamide as a yellow solid (710 mg, 33%). 1H NMR (400 MHz, DMSO-d6) δ ppm 2.88 (t, J=8.33 Hz, 2H), 3.39 (t, J=8.15 Hz, 2H), 3.76 (s, 3H), 5.07 (br s, 1H), 6.24 (s, 1H), 6.83 (s, 1H), 6.89-7.02 (m, 2H), 7.40 (s, 1H), 7.50 (q, J=7.69 Hz, 1H), 7.64 (s, 1H), 8.03 (s, 1H), 8.10 (s, 1H), 8.47 (d, J=8.42 Hz, 1H), 10.46 (s, 1H), 11.39 (s, 1H); ESIMS (M+H)+=434.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-052ac989698b45bbae8dac0fee71e5fd
Source noteuspto-grants-2011_07