HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962869Generated: October 30, 2026
Dimethylformamide → HCID 86752688, compound
https://huagongshe.com/reaction/962869
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Benzyl carbazate | HCID 79242 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-(1-((Tert-butoxy)carbonyl)piperidin-4-yl)propanoic acid | HCID 1512540 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Product | HCID 86752688 | HCID 86752688 | — |
Reaction Steps
1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (380 mg) was added to a mixture of the product of step (a) (0.5 g), diisopropylethylamine (0.34 ml), 1-hydroxybenztriazole (333 mg) and DMF (10 ml) at ambient temperature. The mixture was stirred for 5 minutes and benzyl carbazate (325 mg) in DMF (2 ml) was added. The mixture was stirred for 18 hours at ambient temperature. The solvent was removed by evaporation and the residue was partitioned between ice-water (25 ml) containing 1M sodium hydroxide (2 ml) and ethyl acetate (50 ml). The ethyl acetate extract was washed with water (20 ml), 0.25M citric acid solution (20 ml), water (20 ml) and saturated sodium chloride solution (10 ml) and dried (MgSO4). The solvent was removed by evaporation to give benzyl 3-[3-(1-t-butoxy-carbonylpiperidin-4-yl) propanoyl]carbazate as a foam (790 mg); NMR Spectrum (d6 --DMSO) 0.8-1.1 (m, 2H), 1.3-1.5 (m, 12H), 1.6 (br d, 2H), 2.1 (br t, 2H), 2.62 (m, 2H), 3.9 (br d, 2H), 5.07 (s, 2H), 7.32 (s, 5H), 9.08 (s, 1H), 9.6 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05760057 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-a5a2b975493449949a0051a21d853e54 |
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| Source note | uspto-grants-1998_06 |
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