HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852919Generated: October 30, 2026
Ammonium Chloride → Methyl 4-[(6-morpholin-4-yl-pyridazin-3-ylamino)-methyl]-benzoate
https://huagongshe.com/reaction/852919
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-(6-Chloropyridazin-3-yl)morpholine | HCID 321079 | — |
| Reactant | Methyl 4-(aminomethyl)benzoate hydrochloride | HCID 2729253 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Methyl 4-[(6-morpholin-4-yl-pyridazin-3-ylamino)-methyl]-benzoate | HCID 58930537 | 8.2% |
Reaction Steps
To a solution of 64 (2.0 g, 10.0 mmol) and methyl 4-(aminomethyl)benzoate hydrochloride (2.2 g, 11.0 mmol) in i-PrOH (200 mL) was added NH4Cl (2.14 g, 40.0 mmol). The reaction mixture was heated at 150° C. for 72 h and concentrated. The residue was dissolved in water and the aqueous phase was extracted with. \the aqueous phase was separated, treated with 1N NaOH (pH 8) and extracted with EtOAc. The extract was dried over anhydrous Na2SO4, filtered and concentrated. The residue was purified by flash chromatography on silica gel (MeOH/CH2Cl2: 2/98 to 5/95) to afford the title compound 65 (270 mg, 0.82 mmol, 8% yield). 1H NMR: (400 MHz, CDCl3) δ (ppm): 7.97 (d, J=8.0 Hz, 2H), 7.42 (d, J=8.0 Hz, 2H), 6.90 (d, J=9.2 Hz, 1H), 6.69 (d, J=9.2 Hz, 1H), 5.16-5.06 (bs, 1H), 4.67 (s, 2H), 3.90 (s, 3H), 3.82 (t, J=4.8 Hz, 4H), 3.41 (t, J=4.8 Hz, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253204B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-89f41a02d34945428ae3af8a28b1dab5 |
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| Source note | uspto-grants-2007_08 |
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