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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811762Generated: November 2, 2026

Sodium Chloride → HCID 59224699, compound

https://huagongshe.com/reaction/1811762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantTrifluoroacetic acidHCID 6422—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 59224642HCID 59224642—
ReactantHCID 59224649HCID 59224649—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 59224699HCID 5922469982.8%

Reaction Steps

Trifluoroacetic acid (0.67 ml) was added to a dichloromethane (2.0 ml) solution of 5-(2-amino-6-chloropyrimidin-4-yl)-2,4-dimethylbenzoic acid tert-butyl ester (100 mg, 0.33 mmol) obtained in Step 4 of Example 1-1. The mixture was stirred at room temperature for four hours, and then concentrated under reduced pressure. The resulting white solid material was dissolved in N,N-dimethylformamide (1.0 ml), and then diisopropylethylamine (0.105 ml, 0.603 mmol), N-hydroxysuccinimide (38 mg, 0.333 mmol), and 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide hydrochloride (64 mg, 0.335 mmol) were added thereto. The mixture was stirred at room temperature for 5.5 hours, and then an N,N-dimethylformamide (2.0 ml) solution of (3-aminomethyloxetan-3-ylmethyl)tritylamine (160 mg, 0.446 mmol) obtained in Step 1 above was added thereto. The prepared reaction solution was stirred at room temperature for 17 hours. A saturated aqueous sodium chloride solution (20 mL) was added to the reaction solution, and extracted three times with ethyl acetate (20 ml). The extract was sequentially washed three times with a saturated aqueous sodium bicarbonate solution (30 ml) and then three times with a saturated aqueous sodium chloride solution (30 ml). The washed ethyl acetate solution was dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (developing solvent: dichloromethane:methanol=30:1) to yield 5-(2-amino-6-chloropyrimidin-4-yl)-2,4-dimethyl-N-{3-[(tritylamino)methyl]oxetan-3-ylmethyl}benzamide (169 mg) as a white solid material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362236B2
Source datasetuspto-grants-2013_01
ORD IDord-e83bbedde9334c1a87174c4105815b47
Source noteuspto-grants-2013_01