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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718707Generated: October 29, 2026

Tert-butyl 4-bromobenzoate → tert-Butyl 4-(6-chloro-8-morpholino-2-((1R,2S)-2-(quinolin-2-yl)cyclopropyl)imidazo[1,2-b]pyridazin-3-yl)benzoate

https://huagongshe.com/reaction/718707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-bromobenzoateHCID 11334366—
Reactant4-(6-Chloro-2-((1R,2S)-2-(quinolin-2-yl)cyclopropyl)imidazo[1,2-b]pyridazin-8-yl)morpholineHCID 117728491—
Producttert-Butyl 4-(6-chloro-8-morpholino-2-((1R,2S)-2-(quinolin-2-yl)cyclopropyl)imidazo[1,2-b]pyridazin-3-yl)benzoateHCID 131734183—

Reaction Steps

Compound 79d (33 mg, 0.081 mmol) was coupled with tert-butyl 4-bromobenzoate (29 μL, 0.12 mmol) using the procedure described in Example 20, Step A to afford title compound 146. 1H NMR (400 MHz, CD3OD) δ (ppm): 7.93-8.08 (m, 4H), 7.72-7.85 (m, 3H), 7.66 (t, J=7.6 Hz, 1H), 7.41-7.50 (m, 1H), 7.24-7.31 (m, 1H), 6.12 (s, 1H), 4.05 (br. s., 4H), 3.95 (d, J=3.9 Hz, 4H), 2.80-2.93 (m, 2H), 1.87-2.00 (m, 2H), 1.58 (s, 9H) Mass Spectrum (LCMS, ESI pos.): Calcd. for C33H32ClN5O3: 582.2 (M+H). found: 582.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193736B2
Source datasetuspto-grants-2015_11
ORD IDord-4988ef8e173e4b77a0f2c33d0097a30b
Source noteuspto-grants-2015_11