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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57649Generated: October 30, 2026

Tert-butyl 2-((7-(4-morpholinophenyl)pyrido[4,3-b]pyrazin-5-ylamino)methyl)-1,1-dioxo-thiomorpholine-4-carboxylate → 7-(4-morpholinophenyl)-N-(1,1-dioxo-thiomorpholin-2-ylmethyl)pyrido[4,3-b]pyrazin-5-amine

https://huagongshe.com/reaction/57649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 2-((7-(4-morpholinophenyl)pyrido[4,3-b]pyrazin-5-ylamino)methyl)-1,1-dioxo-thiomorpholine-4-carboxylateHCID 86717408—
SolventHydrochloric AcidHCID 313—
SolventEthyl AcetateHCID 8857—
Product7-(4-morpholinophenyl)-N-(1,1-dioxo-thiomorpholin-2-ylmethyl)pyrido[4,3-b]pyrazin-5-amineHCID 8671740977.2%

Reaction Steps

The tert-butyl 2-((7-(4-morpholinophenyl)pyrido[4,3-b]pyrazin-5-ylamino)methyl)-1,1-dioxo-thiomorpholine-4-carboxylate (52 mg, 0.094 mmol) was dissolved in the solution of HCl in ethyl acetate (3 mL), and the mixture was stirred at room temperature for 2 hours until TLC indicated Boc group was removed. The volatile materials was removed, the residue was neutralized with ammonium hydroxide (25%, 1 mL) and purified by C18 column to afford yellow solid 33 mg. MS (m/z): 455 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434726B2
Source datasetuspto-grants-2016_09
ORD IDord-1a7876c106914f51b5faabb6ad118692
Source noteuspto-grants-2016_09