HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114149Generated: October 31, 2026
3-Amino-1-propanol → HCID 69204532, compound
https://huagongshe.com/reaction/2114149
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Amino-1-propanol | HCID 9086 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 5'-(3-Furoylamino)-2'-methyl-1,1'-biphenyl-4-carboxylic acid | HCID 69152146 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 69204532 | HCID 69204532 | 83.5% |
Reaction Steps
5′-(3-Furoylamino)-2′-methyl-1,1′-biphenyl-4-carboxylic acid (30 mg, 0.093 mmol), 3-hydroxypropylamine (7 mg, 0.093 mmol), HATU (35.5 mg, 0.093 mmol), HOBT (12.6 mg, 0.093 mmol) and DIPEA (48 μl, 0.28 mmol) in DMF (2 ml) were stirred at room temperature for 18 h. The reaction was diluted with ethyl acetate (150 ml), washed with water (2×30 ml) and dried (magnesium sulphate). The solvent was evaporated under vacuum and the residue chromatographed on a silica flash column eluting with DCM/methanol/triethylamine (96:2:2). Concentration of the product fractions under vacuum gave N-(4′-{[(3-hydroxypropyl)amino]carbonyl}-6-methyl-1,1′-biphenyl-3-yl)-3-furamide (29.4 mg, 83%). NMR; δH [2H6]—DMSO 9.91,(1H, s), 8.50,(1H, t), 8.35,(1H, s), 7.90,(2H, d), 7.78,(1H, t), 7.66,(1H, dd), 7.59,(1H, d), 7.43,(2H, d), 7.27,(1H, d), 6.97,(1H, m), 4.49,(1H, t), 3.47,(2H, q), 3.33,(2H, m), 2.19,(3H, s), 1.69,(2H, m). LCMS: retention time 2.77 min, MH+379.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432289B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-65e8cd6875ee4e8896dd44176ce00c8c |
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| Source note | uspto-grants-2008_10 |
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