HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651795Generated: October 30, 2026
Benzyloxycarbonylglycine → HCID 86757303, compound
https://huagongshe.com/reaction/651795
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyloxycarbonylglycine | HCID 14349 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 70203736 | HCID 70203736 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86757303 | HCID 86757303 | — |
Reaction Steps
A mixture of 0.257 g of 2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenylbutyl]-4-methyl-N-[2,4-dioxo-1,3,8-triazaspiro[4.5]decan-3-yl]valeramide and 0.209 g of N-(benzyloxycarbonyl)glycine in 5 ml of dry dimethylformamide was stirred and cooled to ice temperature. The mixture was treated with 0.225 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride and was then stirred at room temperature for 2 days. The solvent was evaporated and the residue partitioned between water and ethyl acetate. The ethyl acetate layer was washed successively with water, 5% aqueous sodium bicarbonate solution, saturated sodium chloride solution and dried over anhydrous magnesium sulphate. The solvent was evaporated and the residue triturated with ether and there was obtained 0.261 g of N-[8-{N-(benzyloxycarbonyl)aminoacetyl]-2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenylbutyl]-4-methyl-N-[2,4-dioxo-1,3,8-triazaspiro[4.5]decan-3-yl]valeramide 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-5eb260fc4f3348a8aedc3476a1ab4dfa |
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| Source note | uspto-grants-2001_08 |
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