HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368871Generated: October 31, 2026
HCID 15407200, compound → HCID 517029, compound
https://huagongshe.com/reaction/1368871
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 15407200 | HCID 15407200 | — |
| Reactant | HCID 178449450 | HCID 178449450 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 517029 | HCID 517029 | — |
Reaction Steps
Under an argon atmosphere, a dichloromethane (15 ml) solution of the 2-methyl-1-(3-phenylpropanoylamino)propylphosphinic acid (162 mg) obtained in the above step (a) was added with benzyl (S)-6-benzyloxycarbonylamino-2-hydroxyhexanoate (228 mg) which was obtained from 6-amino-2-hydroxyhexanoic acid described in Chem. Pharm. Bull., 621(1976) in a conventional manner, N-(dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (180 mg), and dimethylaminopyridine (38.7 mg), and then the mixture was stirred at room temperature for 16 hours. The organic substances were extracted with ethyl acetate, and the extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel column chromatography (10 g, chloroform:methanol=10:1) to obtain benzyl (S)-6-(benzyloxycarbonylamino)-2-((2-methyl-1-(3-phenylpropanoylamino)propyl)phosphinoyloxy)hexanoate (117 mg, 31%). This compound was subjected to the measurement of molecular weight and then used in the following reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06576627B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-469341d5de4e4515ac179ab74eda2a85 |
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| Source note | uspto-grants-2003_06 |
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