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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44814Generated: October 25, 2026

Dichloromethane → (7R)-2-chloro-8-(1-cyclopropylethyl)-7-ethyl-5-methyl-7,8-dihydropteridin-6(5H)-one

https://huagongshe.com/reaction/44814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantCyclopropyl methyl ketoneHCID 13004—
Reactant2,4-Dichloro-5-nitropyrimidineHCID 521266—
Reactantmethyl (2R)-2-aminobutanoate hydrochlorideHCID 13283516—
Solvent1,2-DichloroethaneHCID 11—
Product(7R)-2-chloro-8-(1-cyclopropylethyl)-7-ethyl-5-methyl-7,8-dihydropteridin-6(5H)-oneHCID 58405334—

Reaction Steps

Intermediate SS is prepared from compound I-SS via compound II-SS, III-SS and IV-SS similarly to the methods used in preparing compound III-J, Intermediate J-1, compound IV-J and Intermediate J as described above, with (R)-methyl 2-aminobutanoate hydrochloride used instead of (R)-methyl 2-aminobutanoate and with cyclopropylethanone instead of dihydro-2H-pyran-4(3H)-one in the first step, and with PE/dichloromethane instead of PE/1,2-dichloroethane as solvent in the coupling of 2,4-dichloro-5-nitropyrimidine with compound II-SS. Compound III-SS; LCMS: 343.1 m/z (M+H)+. Compound IV-SS; LCMS: 281.1 m/z (M+H)+. Intermediate SS. LCMS: 295 m/z (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541418B2
Source datasetuspto-grants-2013_09
ORD IDord-114beb85103a47df957a572d7b54baf4
Source noteuspto-grants-2013_09