HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116692Generated: November 1, 2026
1,3-Bis(diphenylphosphino)propane → HCID 25008813, compound
https://huagongshe.com/reaction/2116692
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Bis(diphenylphosphino)propane | HCID 81219 | — |
| Reactant | HCID 11513116 | HCID 11513116 | — |
| Catalyst | Rhodium, di-mu-chlorobis((1,2,5,6-eta)-1,5-cyclooctadiene)di- | HCID 6436379 | — |
| Product | HCID 25008813 | HCID 25008813 | — |
Reaction Steps
54 mg (73.0 mmol) 4-(2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-piperidine-1-carboxylic acid-{(R)-1-(4-amino-3-chloro-5-ethynyl-benzyl)-2-[4-(4-methyl-piperazin-1-yl)-piperidin-1-yl]-2-oxo-ethyl}-amide, 10 mg (0.02 mmol) of bis(1,5-cyclooctadiene)-di-rhodium(I)-dichloride, 16.5 mg (0.04 mmol) 1,3-bis(diphenylphosphino)-propane were dissolved in 10 ml degassed methanol and 0.1 ml degassed triethylamine and then hydrogenated for 2 hours at ambient temperature and 3 bar hydrogen pressure. The reaction mixture was evaporated down under reduced pressure and taken up in ethyl acetate. The insoluble precipitate was removed by suction filtering and the filtrate was evaporated down under reduced pressure. The residue was purified by column chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439237B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-9cbe570f575046beabec0a21b4adfd22 |
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| Source note | uspto-grants-2008_10 |
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