Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068877Generated: November 1, 2026

4-Methylmorpholine → HCID 178522644, compound

https://huagongshe.com/reaction/1068877

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
Reactant1,3-Dioxaindane-4-carboxylic acidHCID 304832—
ReactantHCID 178509242HCID 178509242—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178522644HCID 178522644—

Reaction Steps

Under a nitrogen atmosphere, 320 μl (2.9 mmol) of NMM and 210 1 (1.6 mmol) of isobutyl chloroformate are added at −20° C. to 250 mg (1.5 mmol) of 2,3-methylenedioxybenzoic acid [for preparation see: Chem. Ber. 104 (1971) 2347] in 3.2 ml of THF and then stirred for 45 min. 378 mg (1.45 mmol) of 3-amino-4-(3-chloro-phenylamino)-1H-pyrazolo-[3,4-d]pyrimidine (see Step 1.6) are then added and the reaction mixture is allowed to rise to RT and is stirred for 1 hour to complete the reaction. The reaction mixture is poured into 100 ml of water and stirred for 1 hour, and the crude product is filtered off and washed with water and ethanol. Dissolution in 3 ml of DMSO at =110° C., cooling, filtering and washing with ethanol yield 4-(3chloro-phenylamino)-3-(2,3-methylenedioxy-benzoylamino)-1H-pyrazolo[3,4-d]pyrimidine; HPLC:tRet(grad20-100/20)=16.5; FAB-MS: (M+H)+=409.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251911B1
Source datasetuspto-grants-2001_06
ORD IDord-e31252d2d8c445639500f69d5fb1e5c5
Source noteuspto-grants-2001_06