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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405307Generated: October 31, 2026

Tert-Butylamine → (S)-N-tert-butyl-2-(4-fluorophenyl)-3-(2-methylpyrrolidin-1-yl)quinoxaline-6-carboxamide

https://huagongshe.com/reaction/1405307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantTriethylamineHCID 8471—
ReactantPropylphosphonic anhydrideHCID 111923—
Reactant(S)-2-(4-Fluorophenyl)-3-(2-methylpyrrolidin-1-yl)quinoxaline-6-carboxylic acidHCID 50991311—
SolventDichloromethaneHCID 6344—
Product(S)-N-tert-butyl-2-(4-fluorophenyl)-3-(2-methylpyrrolidin-1-yl)quinoxaline-6-carboxamideHCID 70654210—

Reaction Steps

To a solution of (S)-2-(4-fluorophenyl)-3-(2-methylpyrrolidin-1-yl)quinoxaline-6-carboxylic acid (200 mg, 0.57 mmol) in dichloromethane (30 mL) was added 2-methylpropan-2-amine (46 mg, 0.63 mmol), triethylamine (115 mg, 1.14 mmol) and T3P (217 mg, 0.68 mmol) dropwise with stifling. The resulting solution was stirred for 3 h at room temperature and then concentrated in vacuo to afford (S)—N-tert-butyl-2-(4-fluorophenyl)-3-(2-methylpyrrolidin-1-yl)quinoxaline-6-carboxamide as a yellow oil (160 mg, crude).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916561B2
Source datasetuspto-grants-2014_12
ORD IDord-89b2f7bc7fcd49369e2e939f57fd2d4c
Source noteuspto-grants-2014_12