HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470342Generated: October 30, 2026
4-Methylmorpholine → HCID 56848566, compound
https://huagongshe.com/reaction/1470342
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 2-Amino-2-methyl-1-propanol | HCID 11807 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 66778978 | HCID 66778978 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 56848566 | HCID 56848566 | 42% |
Reaction Steps
3-Methyl-5-(7-phenyl-furo[3,2-b]pyridin-2-yl)-benzoic acid (79 μmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimidhydrochlorid (86,592 μmol) are dissolved in N,N-dimethylformamid (300.00 μl) and 4-methylmorpholin (157.354 μmol) and 1-hydroxybenzotriazolhydrat (86.849 μmol) are added and stirred 5 min at RT. A solution of 2-amino-2-methyl-propan-1-ol (80,000 μmol) in N,N-dimethylformamid (100.00 μl) is added. The mixture is stirred 4.5 h at RT. The reaction solution is poured into water and extracted with ethylacetate. The combined organic layers are dried over MgSO4 and the solvent is removed in vacuo. The product is isolated after reversed phase column chromatography as yellow solid (33 μmol, 42% yield). HPLC (method A): Rt 2.55 min (purity 98.5%); LCMS (ESI+) (method E): Rt 2.199 min, M+H+401.1 m/z; 1H NMR (500 MHz, DMSO-d6) δ [ppm] 8.60 (d, J=5.1, 1H), 8.18 (s, 1H), 8.16-8.10 (m, 2H), 7.96 (s, 1H), 7.77 (s, 1H), 7.70 (d, J=8.9, 2H), 7.65 (dd, J=14.7, 6.4, 3H), 7.58 (d, J=7.4, 1H), 4.16 (br, 1H), 3.54 (s, 2H), 2.47 (s, 3H), 1.35 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006440B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-aa5e00a369754f06a093588d765f54d1 |
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| Source note | uspto-grants-2015_04 |
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