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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528023Generated: October 30, 2026

Sodium Hydroxide → HCID 66799957, compound

https://huagongshe.com/reaction/528023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 66799891HCID 66799891—
ReactantHCID 66799955HCID 66799955—
SolventMethanolHCID 887—
ProductHCID 66799957HCID 66799957—

Reaction Steps

9-Cyclopropyl-6-[4-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidin-1-yl]-9H-purine-8-carboxylic acid was prepared in the same manner as 9-methyl-6-[4-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidin-1-yl]-9H-purine-8-carboxylic acid. The 8-cyclopropyl-6-methoxy-4-[4-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidin-1-yl]pteridin-7(8H)-one (0.836 g, 1.93 mmol) was treated with 2M sodium hydroxide (10 mL, 20 mmol) in methanol at 80° C. for 18 hours gave 0.789 of 9-cyclopropyl-6-[4-(2-oxo-2,3-dihydro-1H-benzimidazol-1-yl)piperidin-1-yl]-9H-purine-8-carboxylic acid as an off-white solid. 1H NMR (400 MHz, DMSO-d6): δ 11.20 (br s, 1H), 8.07 (s, 1H), 6.93 (m, 1H), 6.71 (m, 3H), 5.19 (broad s, 2H), 4.27 (m, 1H), 3.40 (m, 2H), 3.19 (t, 2H), 2.43 (m, 2H), 1.82 (d, 2H), 1.15 (m, 2H), 0.84 (m, 2H). MS (EI) for C21H21N7O4: 420 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346807B2
Source datasetuspto-grants-2016_05
ORD IDord-66155002b44b49178e6c1c87c50a5110
Source noteuspto-grants-2016_05