HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251180Generated: October 31, 2026
Methyl bromoacetate → HCID 67272256, compound
https://huagongshe.com/reaction/251180
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Bis-(3-methyl-pyridin-2-ylmethyl)-piperidin-4-yl-amine | HCID 58996965 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67272256 | HCID 67272256 | 83.4% |
Reaction Steps
To a 0° C. solution of a solution of COMPOUND 249 (150 mg, 0.483 mmol) in CH2Cl2 (10 mL) and DIPEA (0.170 mL, 0.966 mmol) was added methyl bromoacetate (0.055 mL, 0.579 mmol), and the reaction mixture was stirred for 17 hr at room temperature. Saturated NaHCO3 (10 mL) was added to the reaction mixture, which was then extracted with CH2Cl2 (3×30 mL). The combined organic extracts were dried (MgSO4), filtered and concentrated. The residue was purified by radial chromatography on silica gel (20:1:0.5 CH2Cl2:MeOH:NH4OH) to give {4-[bis-(3-methyl-pyridin-2-ylmethyl)-amino]-piperidin-1-yl}-acetic acid methyl ester (154 mg, 83%). 1H NMR (CDCl3) δ 1.86-1.92 (m, 4H), 1.98-2.07 (m, 2H), 2.08 (s, 6H), 2.45-2.50 (m, 1H), 2.96-2.99 (m, 2H), 3.17 (s, 2H), 3.71 (s, 3H), 3.83 (s, 4H), 7.07 (dd, 2H, J=4.8, 7.5 Hz), 7.34 (d, 2H, J=7.5 Hz), 8.33 (d, 2H, J=4.8 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863293B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-ad5748f27f48419d833bf4b15b25fe3e |
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| Source note | uspto-grants-2011_01 |
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