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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511007Generated: October 29, 2026

Acetic Acid → HCID 178492203, compound

https://huagongshe.com/reaction/511007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantMorpholineHCID 8083—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 18627201HCID 18627201—
ReactantHCID 86666922HCID 86666922—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178492203HCID 17849220335.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 3-chloro-2-fluoro-6-methoxy-5-(1-{[9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl]amino}ethyl)benzaldehyde (10 mg, 0.023 mmol), in THF (0.95 mL) was stirred at 40° C. for 1 hour. Sodium triacetoxyborohydride (15 mg, 0.069 mmol) and acetic acid (50 μL, 0.88 mmol) were added and the mixture was stirred at 40° C. overnight. Morpholine (20 μL, 0.23 mmol) and sodium cyanoborohydride (14 mg, 0.23 mmol) were added and the mixture was heated at 40° C. for 1 hour. The solvents were stripped down and few drops of trifluoroacetic acid/THF solution (1:1) were added and the mixture stirred for 30 minutes. The mixture was treated with 6.0 M HCl in water (0.5 mL, 3 mmol) for 30 minutes. Purification by preparative LCMS (pH 10) gave the desired compound (3.4 mg, 35%). LCMS calculated for C19H23ClFN6O2 (M+H)+: m/z=421.2. found: 421.1. 1H NMR (DMSO-d6, 500 MHz) δ 12.91 (1H, br s), 8.17 (2H, m), 7.72 (1H, m), 5.89 (1H, br s), 4.05 (3H, s), 3.50 (7H, m), 2.41 (4H, m), 1.42 (3H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-95ffa973034a466d83a9a78b5170f2b7
Source noteuspto-grants-2015_08