HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156951Generated: November 2, 2026
Dicyclohexylcarbodiimide → BOC-(D)-Asn-Gly-MePhe-NHNHCSNH2
https://huagongshe.com/reaction/1156951
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dione | HCID 89529 | — |
| Reactant | Boc-D-asparagine | HCID 1623168 | — |
| Reactant | HCID 12802635 | HCID 12802635 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | BOC-(D)-Asn-Gly-MePhe-NHNHCSNH2 | HCID 12802643 | — |
Reaction Steps
In 10 ml of trifluoroacetic acid is dissolved 0.80 g of BOC-Gly-MePhe-NHNHCSNH2 and the solution is shaken for 10 minutes, concentrated, treated with ether and filtered to obtain a powder. This powder is dissolved in 10 ml of DMF, and after ice-cooling, the solution is neutralized with 0.20 ml of TEA followed by addition of 0.47 g of BOC-(D)-Asn-OH, 0.40 g of HONB and 0.45 g of DCC. The mixture is stirred for 20 hours, the precipitated DCU filtered off, the solvent distilled off and the residue dissolved in n-butanol. The solution is washed with a saturated aqueous solution of sodium hydrogen carbonate and water in that order and dried over anhydrous sodium sulfate. The solvent is distilled off and the residue is treated with ether and filtered to obtain a powder, which is further reprecipitated from methanol-ether. Yield 0.69 g; m.p. 124°-127° C.; [α]D24 -42.5° (c=1.0, DMF); Rf1 0.16.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04337247 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-f4fbd834bdee40638a0179a2ed702840 |
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| Source note | uspto-grants-1982_06 |
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