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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946808Generated: October 31, 2026

6-[(Cyclopropylmethyl)(propyl)amino]pyrimidine-4-carboxylic acid → HCID 67528819, compound

https://huagongshe.com/reaction/1946808

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-[(Cyclopropylmethyl)(propyl)amino]pyrimidine-4-carboxylic acidHCID 59447000—
Reactanttert-butyl 5-amino-3-(3-methoxy-3-oxopropyl)-1H-indazole-1-carboxylateHCID 59447029—
SolventDichloromethaneHCID 6344—
ProductHCID 67528819HCID 67528819—

Reaction Steps

A solution of 6-((cyclopropylmethyl)(propyl)amino)pyrimidine-4-carboxylic acid (Intermediate 21, 31 mg; 0.13 mmol) in DCM (5 ml) was treated with tert-butyl 5-amino-3-(3-methoxy-3-oxopropyl)-1H-indazole-1-carboxylate (Intermediate 45, 35 mg; 0.11 mmol) and polymer-supported Mukaiyama reagent (300 mg). After stirring at RT for 3 hours the mixture was filtered and washed with water. The organic phase was passed through a hydrophobic frit and the solvent removed in vacuo. The residue was purified by column chromatography (silica) eluting with petroleum ether containing increasing amounts of EtOAc to give tert-butyl 5-(6-((cyclopropylmethyl)(propyl)amino)pyrimidine-4-carboxamido)-3-(3-methoxy-3-oxopropyl)-1H-indazole-1-carboxylate. The intermediate was redissolved in DCM (2 ml) and treated with TFA (1 ml) and water (1 drop). After stirring at RT for 3 hours the solvent was removed in vacuo. The residue was partitioned between DCM and saturated sodium bicarbonate solution. The separated organic phase was passed through a hydrophobic frit and the solvent removed in vacuo. The residue was purified by column chromatography (silica) eluting with petroleum ether containing increasing amounts of EtOAc to give the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399448B2
Source datasetuspto-grants-2013_03
ORD IDord-e5c102ecaf764f119a341a130f289c9b
Source noteuspto-grants-2013_03