HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895790Generated: November 1, 2026
Trimethylsilyl triflate → HCID 86675865, compound
https://huagongshe.com/reaction/1895790
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67960504 | HCID 67960504 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86675865 | HCID 86675865 | 100% |
Reaction Steps
A solution of (S)-1-{(S)-2-((S)-2-tert-butoxycarbonylamino-3-methyl-butyrylamino)-3-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-propionyl}-hexahydro-pyridazine-3-carboxylic acid 4-vinyl-pyridin-2-ylmethyl ester (377 mg, 0.52 mmol) in dichloromethane (10 mL) was stirred at 0° C. under nitrogen. Trimethylsilyl trifluoromethanesulfonate (173 mg, 0.14 mL, 0.78 mmol) was added and the reaction mixture was stirred at 0° C. for 1 hour. N,N-Diisopropylethylamine (268 mg, 0.36 mL, 2.08 mmol) was added and the reaction mixture was warmed to room temperature. The solvent was evaporated to afford (S)-1-[(S)-3-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-((S)-2-formylamino-3-methyl-butyrylamino)-propionyl]-hexahydro-pyridazine-3-carboxylic acid 4-vinyl-pyridin-2-ylmethyl ester (0.52 mmol), which was used crude in the next step. LCMS (m/z) 624 [M+H], Tr=4.30 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513184B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-73672f1636904c8d9ce7fd85d15b9c9a |
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| Source note | uspto-grants-2013_08 |
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