HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877177Generated: October 30, 2026
Hydrochloric Acid → HCID 58136535, compound
https://huagongshe.com/reaction/877177
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | Methyl 4-(aminomethyl)benzoate hydrochloride | HCID 2729253 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 58136554 | HCID 58136554 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58136535 | HCID 58136535 | — |
Reaction Steps
60 mg (0.127 mmol) of (4-{[4-(4-chlorophenyl)-1-oxophthalazin-2(1H)-yl]methyl}phenyl)(cyclopentyl)acetic acid (Example 65A) were dissolved in 0.6 ml of dichloromethane, and 26 mg (0.127 mmol) of methyl 4-(aminomethyl)benzenecarboxylate hydrochloride, 19 mg (0.140 mmol) of 1-hydroxy-1H-benzotriazole hydrate, 28 mg (0.146 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 28 mg (0.273 mmol) of triethylamine were added in succession. The reaction mixture was stirred at room temperature overnight. 1 N hydrochloric acid was then added, and the mixture was extracted with ethyl acetate. The combined organic phases were dried over sodium sulfate and concentrated on a rotary evaporator. The residue was purified by preparative HPLC. This gave 36 mg (46% of theory) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987256B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-465a74a2e73e4955bde7ad01865ba892 |
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| Source note | uspto-grants-2015_03 |
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