HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655737Generated: October 31, 2026
Diisopropylethylamine → HCID 178456002, compound
https://huagongshe.com/reaction/1655737
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | HCID 53649524 | HCID 53649524 | — |
| Reactant | HCID 178456019 | HCID 178456019 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178456002 | HCID 178456002 | 66.7% |
Reaction Steps
100 mg (0.256 mmol) of (S)-α-amino-N-[(1S,2S,4S)-1-(cyclohexylmethyl)-2-hydroxy-4-isopropyl-5-hexenyl]-imidazole-4-propionamide and 0.052 ml of Hunig base in 2 ml of acetonitrile were treated at room temperature with 100 mg of N-(dibenzylcarbamoyl)-3-phenyl-L-alanine and 113 mg of BOP and subsequently stirred at room temperature for 12 hours. Thereafter, the reaction solution was poured onto 1N hydrochloric acid/ice, extracted with ethyl acetate, the extracts were dried over sodium sulfate and the solvent was removed under reduced pressure. Chromatography of the residue on silica gel using a 10:1 mixture of methylene chloride and methanol as the eluting agent yielded 130 mg of 1,1-dibenzyl-3-[(S)-α-[[(S)-1-[[(1S,2S,4S)-1-(cyclohexylmethyl)-2-hydroxy-4-isopropyl-5-hexenyl]carbamoyl]-2-imidazol-4-ylethyl]carbamoyl]phenethyl]urea in the form of an amorphous solid. MS: 761 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05250517 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-b252782c8a7f49fcad0c2e6d69760bef |
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| Source note | uspto-grants-1993_10 |
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