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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600404Generated: October 29, 2026

Trimethyl orthoformate → HCID 59799574, compound

https://huagongshe.com/reaction/600404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
ReactantHCID 86622936HCID 86622936—
CatalystMethanesulfonic AcidHCID 6395—
SolventMethanolHCID 887—
ProductHCID 59799574HCID 5979957473%

Reaction Steps

Pale yellow solid. Synthesized from 2-(2-amino-5-fluorophenylamino)-6-chloro-9-(tetrahydro-2H-pyran-4-yl)-7H-purin-8(9H)-one (160 mg, 0.42 mmol) in anhydrous methanol (10 mL), using anhydrous trimethylorthoformate (1 mL) and methane sulfonic acid (5 drops) with stirring under Ar at room temperature for 2 h (HPLC monitoring). The solvent was removed in vacuo and the residue purified by column chromatography (silica gel, gradual elution with 2% methanol in methylene chloride to 10% methanol in methylene chloride) to afford the desired product (120 mg, 73% yield). 1H NMR (300 MHz, CDCl3+CD3OD) δ, ppm: 9.03 (s, 1H), 8.40-8.20 (m, 1H), 7.82-7.72 (m, 1H), 7.17-7.11 (m, 1H), 4.72-4.58 (m, 1H), 4.28-4.13 (m, 2H), 3.70-3.62 (m, 2H), 2.90-2.72 (m, 2H), 1.90-1.78 (m, 2H); MS (EI) m/z 389.2 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902187B2
Source datasetuspto-grants-2011_03
ORD IDord-b84225db2d0f4b27acec28ca4cd049b3
Source noteuspto-grants-2011_03