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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283855Generated: November 1, 2026

Triethylamine → HCID 66958605, compound

https://huagongshe.com/reaction/2283855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-hydroxybenzenecarboximidoyl chlorideHCID 2756315—
ReactantHCID 86604924HCID 86604924—
SolventDichloromethaneHCID 6344—
ProductHCID 66958605HCID 6695860580%

Reaction Steps

α-Chlorobenzaldoxime (0.64 g, 4.1 mmol) was added to a solution of di(tert-butyl) 1-pent-4-ynyl-2-propyl-2H-pyrazolo[3,4-c]quinolin-4-ylimidodicarbonate (prepared as described in Parts A-E of Example 57, 1.36 g, 2.76 mmol) and triethylamine (0.60 mL, 4.14 mmol) in dichloromethane (10 mL). The solution was heated at 40° C. for 19 hours, during which time additional α-chlorobenzaldoxime (0.65 g) was added. The reaction was worked up as described in Part B of Example 595. The crude product was purified by chromatography (silica gel, sequential elution with 20% then 40% ethyl acetate in hexanes) to provide 1.35 g of di(tert-butyl) 1-[3-(3-phenylisoxazol-5-yl)propyl]-2-propyl-2H-pyrazolo[3,4-c]quinolin-4-ylimidodicarbonate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145410B2
Source datasetuspto-grants-2015_09
ORD IDord-9a09813f719b452eac01698a212aff65
Source noteuspto-grants-2015_09