HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735508Generated: October 30, 2026
Dicyclohexylcarbodiimide → HCID 22879396, compound
https://huagongshe.com/reaction/1735508
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | (1S,2R,3S)-3-amino-4-cyclohexyl-1-cyclopropyl-1,2-butanediol | HCID 14930738 | — |
| Reactant | HCID 22862631 | HCID 22862631 | — |
| Catalyst | N-Hydroxysuccinimide | HCID 80170 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22879396 | HCID 22879396 | 87.2% |
Reaction Steps
89 g (170 mmol) of (S)-1-(t-butoxycarbonyl)-α-[(S)-α-[(t-butylsulphonyl)methyl]hydrocinnamamido]imidazole-4-propionic acid, 1 g (8.5 mmol) of N-hydroxysuccinimide, 35.5 g (155 mmol) of (1S,2R,3S)-3-amino-4-cyclohexyl-1-cyclopropyl-butane-1,2-diol and 800 ml of ethyl acetate were stirred at 20°. A solution of 37 g (178 mmol) of dicyclohexylcarbodiimide in 110 ml of ethyl acetate was added within 10 minutes. The reaction had finished after stirring at 20° for 17 hours. The solid (dicyclohexylurea) was filtered off and the filtrate was treated while stirring firstly with 68 ml of deionized water and then with 1100 ml of hexane. After one hour at 0° the crystallizate was filtered off under suction and triturated in methanol at 20°. The suspension was cooled to -15° and the product was filtered off. 98.8 g (86%) of t-butyl 4-[(S)-2 -[(S)-2-t-butanesulphonylmethyl-3-phenylpropionylamino]-2-[(1S,2R,3S)-1-cyclohexylmethyl-3-cyclopropyl-2,3-dihydroxy-propylcarbamoyl]ethyl]-1H-imidazole-1-carboxylate were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05536816 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-b964d0c4d49a4fbf9e5e21e9c4f34bc7 |
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| Source note | uspto-grants-1996_07 |
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