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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42348Generated: October 26, 2026

Diisopropylethylamine → HCID 178461982, compound

https://huagongshe.com/reaction/42348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantAcetonitrile--water (1/1)HCID 18373917—
Reactant(R)-4-(1-aminoethyl)-N-tert-butylbenzenesulfonamideHCID 28714635—
ReactantHCID 178517814HCID 178517814—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178461982HCID 178461982162.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-chloro-6-(4-fluorophenyl)pyrido[3,2-d]pyrimidin-4-ol (377 mg), (R)-4-(1-aminoethyl)-N-tert-butylbenzenesulfonamide (456 mg) and DIEA (243 ml) in NMP (4 ml) was heated at 120° C. overnight. The reaction mixture was then added to H2O/ACN (9:1) with vigorous stirring and extracted with EtOAc. The organic layer was dried and concentrated to give 1.1 g crude (R)—N-tert-butyl-4-(1-(6-(4 fluorophenyl)-4-hydroxypyrido[3,2-d]pyrimidin-2-ylamino)ethyl)benzenesulfonamide as golden brown oil, which was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536187B2
Source datasetuspto-grants-2013_09
ORD IDord-d2f8bc44125c4c279e602f75ded9a355
Source noteuspto-grants-2013_09