HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651778Generated: October 31, 2026
Fmoc-Gly-OH → (E)-2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenyl-3-butenyl]-2'-[N-(9-fluorenylmethyloxycarbonyl)-glycinyl]-4-methylvalerohydrazide
https://huagongshe.com/reaction/651778
Participants
| Role | Name | HCID | Charge |
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| Reactant | Fmoc-Gly-OH | HCID 93124 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | (E)-2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenyl-3-butenyl]-4-methylvalerohydrazide | HCID 69709501 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (E)-2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenyl-3-butenyl]-2'-[N-(9-fluorenylmethyloxycarbonyl)-glycinyl]-4-methylvalerohydrazide | HCID 86757289 | 86.8% |
Reaction Steps
A solution of 1.0 g of (E)-2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenyl-3-butenyl]-4-methylvalerohydrazide in 10 ml of dimethylformamide was treated with 1.24 g of N-(9-fluorenylmethyloxycarbonyl)-glycine and 0.80 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride. The mixture was stirred overnight at room temperature and evaporated. The residue was dissolved in ethyl acetate and washed with 2M aqueous hydrogen chloride, 5% aqueous sodium hydrogen carbonate and saturated aqueous sodium chloride. Drying over anhydrous magnesium sulphate followed by evaporation and trituration with diethyl ether gave 1.54 g of (E)-2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenyl-3-butenyl]-2′-[N-(9-fluorenylmethyloxycarbonyl)-glycinyl]-4-methylvalerohydrazide in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06281363B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-3086874a427944d0ae4988e6328897ec |
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| Source note | uspto-grants-2001_08 |
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