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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566407Generated: October 31, 2026

Hydrochloric Acid → HCID 44532110, compound

https://huagongshe.com/reaction/566407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
ReactantEthanamine, 2-(methylsulfonyl)-, hydrochloride (1:1)HCID 17749886—
ReactantHCID 69890959HCID 69890959—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 44532110HCID 44532110—

Reaction Steps

5-[4-(1-Benzyl-1H-indazol-5-ylamino)-pyrido-[3,4-d]pyrimidin-6-yl]-furan-2-carboxylic acid hydrochloride (0.125 g, 0.25 mmol) and carbonyl diimidazole (0.052 g, 0.33 mmol) were suspended in dry THF (3 ml) under a nitrogen atmosphere and stirred at room temperature for 7 hours. 2-(Methanesulphonyl)ethylamine hydrochloride (0.080 g, 0.50 mmol) and triethylamine (0.15 ml, 0.11 g, 1.08 mmol) were added, together with further THF (2 ml), and the resulting mixture was stirred at room temperature for 18 hours. The mixture was absorbed onto silica gel and purified by column chromatography, eluting with 2-10% MeOH/DCM. Concentration of the relevant fractions gave a pale yellow solid. This was resuspended in methanol and treated with ethanolic HCl to give the product as an orange solid, which was collected by filtration, washed with methanol, acetone and ether, and dried in vacuo (0.093 g, 0.154 mmol, 61%); δH [2H6]DMSO 12.00(1H,s), 9.76(1H,s), 9.19-9.29 (2H,m), 8.75 (1H,s), 8.28 (1H,s), 8.22 (1H,s), 7.78-7.90 (2H,m), 7.23-7.38 (7H,m), 5.71 (2H,s), 3.50-3.90 (2H obscured by water signal), 3.48 (2H,t), 3.07 (3H,s); m/z (M+1+) 568.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174889B1
Source datasetuspto-grants-2001_01
ORD IDord-5275a119d4b24265a987c5b57df78334
Source noteuspto-grants-2001_01