HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270996Generated: November 3, 2026
1-Pyrrolidineethanamine → HCID 11272398, compound
https://huagongshe.com/reaction/1270996
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Pyrrolidineethanamine | HCID 1344 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | (S)-3-(Boc-amino)-4-phenylbutyric acid | HCID 2761538 | — |
| Reactant | HCID 69429341 | HCID 69429341 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 11272398 | HCID 11272398 | 84% |
Reaction Steps
[(S)-1-Benzyl-2-(2-pyrrolidin-1-yl-ethylcarbamoyl)-ethyl]-carbamic acid tert-butyl ester. HOBT (0.318 g, 2.36 mmol) and EDCl (0.452 g, 2.36 mmol) were added to a solution of (S)-3-tert-butoxycarbonylamino-4-phenyl-butyric acid (0.27 g, 2.36 mmol) in DMF (16 mL). Following the addition of a solution of 2-pyrrolidin-1-yl-ethylamine (0.44 g, 1.6 mmol) in DMF (2 mL), N-methyl-morpholine (0.32 g, 3.16 mmol) was added dropwise. The reaction mixture was stirred at rt overnight. Water (30 mL) and EtOAc (50 mL) were then added to the mixture. The aqueous layer was extracted with EtOAc (3×50 mL). The combined organic layers were washed with 1 N NaOH (2×40 mL) and brine (50 mL), dried (MgSO4), and concentrated. Purification by column chromatography [0–20% (1% NH4OH/MeOH)/CH2Cl2] afforded 0.5 g (84%) of the desired product. MS (electrospray): mass calculated for C21H33N3O3, 375.25; m/z found, 376.2 [M+H]+. 1H NMR (400 MHz, CDCl3): 7.32–7.21 (m, 5H), 6.22 (s, 1H), 5.78 (s, 1H), 4.14–4.06 (m, 1H), 3.40 (d, J=5.3 Hz, 2H), 3.02–3.00 (m, 1H), 2.83–2.77 (m, 1H), 2.63 (s, 2H), 2.57 (s, 3H), 2.41 (dd, J=14.5, 4.3 Hz, 1H), 2.27 (dd, J=14.5, 5.03 Hz, 1H), 1.82 (s, 4H), 1.43 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202269B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-c3b34da978ef443793e157b613061b19 |
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| Source note | uspto-grants-2007_04 |
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