HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584094Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 54273654, compound
https://huagongshe.com/reaction/1584094
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)- | HCID 85083 | — |
| Reactant | 3-Hydroxypyrrolidine-2,5-dione | HCID 18183696 | — |
| Reactant | 4-(AMINOMETHYL)-3-METHOXYBENZONITRILE | HCID 18424090 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54273654 | HCID 54273654 | 65% |
Reaction Steps
16.0 g of Boc-proline (50 mmol), dissolved in 80 ml of THF, were stirred with 5.7 g of hydroxysuccinimide and 10.2 g of DCC in methylene chloride at 0° C. for 30 min. Then 8.0 g (50 mmol) of 4-aminomethyl-3-methoxybenzenenitrile [sic] dissolved in 50 ml of THF were added dropwise at 0° C., and the mixture was stirred at room temperature for 20 h. The solid was filtered off, the filtrate was mixed with the same volume of ethyl acetate and washed with cooled 5% strength NaHSO4 solution and saturated NaCl solution. 11.5 g (65%) of product were obtained. 1H-NMR (DMSO-d6 ; δ in ppm): 8.38 (m, NH); 7.50-7.35 (m, 3H); 4.40-4.05 (m, 3H, N--CH2 --Ar/N--CH--CO); 3.87 (s, OCH3); 3.50-3.25 (m, 2H, N--CH2); 2.2.5-2.00 [sic] (m, 1H); 1.90-1.65 (m, 3H); 1.40 and 1.30 (2s; 9H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05932567 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-85befb9b04874ab6909d205eaac6a8f0 |
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| Source note | uspto-grants-1999_08 |
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