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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181817Generated: October 30, 2026

O-Methylhydroxylamine hydrochloride → HCID 58980992, compound

https://huagongshe.com/reaction/1181817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
Reactant5-chloro-1H-indole-3-carbaldehydeHCID 2795374—
Reactant4-Acetyl-1-methyl-1H-pyrrole-2-carbaldehydeHCID 12676268—
Reactant6-hydrazino-1-isobutyl-3-methyl-2,4(1H,3H)-pyrimidinedioneHCID 19356084—
Reactant3-(4-acetyl-1-methyl-1H-pyrrol-2-yl)-2-[(5-chloro-1H-indol-3-yl)methyl]-7-isobutyl-5-methyl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dioneHCID 58981140—
ProductHCID 58980992HCID 58980992—

Reaction Steps

This compound was made following the procedure described above, starting with 6-hydrazino-1-isobutyl-3-methylpyrimidine-2,4(1H,3H)-dione, and condensing first 5-chloro-1H-indole-3-carbaldehyde, followed by 4-acetyl-1-methyl-1H-pyrrole-2-carbaldehyde. To the isolated 3-(4-acetyl-1-methyl-1H-pyrrol-2-yl)-2-[(5-chloro-1H-indol-3-yl)methyl]-7-isobutyl-5-methyl-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione was added 4 equivalents of methoxyamine hydrochloride, triethylamie and heated at 80° C. in N,N′dimethylacetamide for 4 h. The mixture was stirred at room temperature for 4 h. The crude reaction product was purified by semi-prep RPHPLC eluting with water/acetonitrile/trfluoroacetic acid mixtures. 536.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285558B2
Source datasetuspto-grants-2007_10
ORD IDord-59c4bf4616584582a3a2caa3a4351445
Source noteuspto-grants-2007_10