Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278339Generated: October 30, 2026

Diisopropylethylamine → US12358901, Example RE6

https://huagongshe.com/reaction/2278339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTriphosgeneHCID 94429—
ReactantMethyl 2-aminoisobutyrate hydrochlorideHCID 13258034—
Reactant6-(7-methylspiro[2H-benzofuran-3,1'-cyclopropane]-4-yl)oxypyridin-3-amineHCID 67959939—
SolventDichloromethaneHCID 6344—
ProductUS12358901, Example RE6HCID 57411298—

Reaction Steps

To a solution of triphosgene (30 mg, 0.1 mmol) in dry DCM (1 ml) at 0° C., under nitrogen atmosphere, DIPEA (0.175 ml, 1.0 mmol) was added followed by the addition (slowly added) of a solution of 6-(7-methylspiro[2H-benzofuran-3,1′-cyclopropane]-4-yl)oxypyridin-3-amine (Intermediate 15, 27 mg, 0.1 mmol) in dry DCM (2 ml) and the reaction mixture was stirred for 15 minutes at the same temperature. After that a solution of Methyl 2-amino-2-methylpropanoate hydrochloride (30 mg, 0.2 mmol) in dry DCM (2 ml) was added and the reaction mixture was stirred for 30 minutes at 0° C. The reaction was quenched with a 1M aqueous solution of HCl (5 ml), diluted with DCM (10 ml) and two phases were separated. The organic layer was washed with brine (10 ml), dried (Na2SO4), filtered and evaporated affording the urea intermediate as yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133175B2
Source datasetuspto-grants-2015_09
ORD IDord-d5177574d7aa4b7094c553e96619b1a7
Source noteuspto-grants-2015_09