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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60224Generated: October 30, 2026

Lithium Hexamethyldisilazide → HCID 58364995, compound

https://huagongshe.com/reaction/60224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-Benzenesulfonyl-5-fluoro-2-{[cyanomethyl-(toluene-4-sulfonyl)amino]-methyl}-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid methyl esterHCID 58365053—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58364995HCID 5836499575.2%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Lithium bis(trimethylsilyl)amide (100 mL of a 1N solution in THF, 100 mmol) was added dropwise to a cooled (−78° C.) suspension of 1-benzenesulfonyl-5-fluoro-2-{[cyanomethyl-(toluene-4-sulfonyl)amino]methyl}-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid methyl ester (16.5 g, 29.6 mmol) in dry THF (150 mL). The reaction mixture was allowed to slowly warm to −10° C. then slowly quenched into cold 1M hydrochloric acid. The layers were separated and the aqueous layer further extracted with THF. The combined organic layer was washed with brine, dried (Na2SO4), filtered and evaporated. The resultant residue was triturated with methanol then acetone and air dried to afford the title compound as a brown solid (8.2 g, 75%). 1H NMR (400 MHz, DMSO-d6): 9.25 (s, 1H), 8.76 (dd, J=2.8, 1.3 Hz, 1H), 8.50 (dd, J=8.2, 2.8 Hz, 1H), 8.20-8.17 (m, 2H), 7.75-7.75 (m, 1H), 7.63-7.62 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440976B2
Source datasetuspto-grants-2016_09
ORD IDord-b81ef6dcbf8c407791fe965b5dcf72d2
Source noteuspto-grants-2016_09