Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854840Generated: October 25, 2026

N-methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)aniline → Methyl 1-cyclopropyl-9-methyl-8-(4-(methylamino)-phenyl)-4-oxo-4H-quinolizine-3-carboxylate

https://huagongshe.com/reaction/1854840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 11957892—
ReactantMethyl 8-chloro-1-cyclopropyl-9-methyl-4-oxo-quinolizine-3-carboxylateHCID 86696543—
ProductMethyl 1-cyclopropyl-9-methyl-8-(4-(methylamino)-phenyl)-4-oxo-4H-quinolizine-3-carboxylateHCID 8669655889.4%

Reaction Steps

Methyl 1-cyclopropyl-9-methyl-8-(4-(methylamino)-phenyl)-4-oxo-4H-quinolizine-3-carboxylate was prepared according to General Procedure A using methyl 8-chloro-1-cyclopropyl-9-methyl-4-oxo-4H-quinolizine-3-carboxylate (74 mg, 0.25 mmol) and N-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-aniline (71 mg, 0.31 mmol). Purification by flash silica column chromatography (CH2Cl2:MeOH) (1:0 to 94:6) afforded the title compound as a yellow solid (81 mg, 81%). ESI-MS m/z: 363 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962842B2
Source datasetuspto-grants-2015_02
ORD IDord-1f3bf5b5dff7442bb6b2b3fc9b58a6ff
Source noteuspto-grants-2015_02