HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926038Generated: October 30, 2026
Methoxyacetic Acid → HCID 57597213, compound
https://huagongshe.com/reaction/1926038
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methoxyacetic Acid | HCID 12251 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 57597331 | HCID 57597331 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 57597213 | HCID 57597213 | 54.9% |
Reaction Steps
A solution of 6-(4-aminophenyl)-N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-5H-pyrrolo[3,2-d]pyrimidin-4-amine (100 mg), methoxyacetic acid (29.4 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (94 mg), 1-hydroxybenzotriazole monohydrate (75 mg) and triethylamine (0.23 mL) in N,N-dimethylformamide (5 mL) was stirred at room temperature for 20 hrs. Methoxyacetic acid (29.4 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (94 mg) and 1-hydroxybenzotriazole monohydrate (75 mg) were added to the reaction system, and the mixture was further stirred for 24 hrs. Water was added to the reaction system and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate and concentrated under reduced pressure, and the residue was separated and purified by column chromatography (basic silica gel, eluent, ethyl acetate→4 methanol:ethyl acetate=14:85) to give the title compound (63.5 mg) as pale-brown powder crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178543B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-76003469d637429ea81b6022cf4c005f |
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| Source note | uspto-grants-2012_05 |
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