HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708387Generated: October 29, 2026
Trifluoroacetic acid → HCID 118379828, compound
https://huagongshe.com/reaction/708387
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 118380252 | HCID 118380252 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 118379828 | HCID 118379828 | 24.4% |
Reaction Steps
Followed the general procedure for the acid mediated deprotection using (3S,4R)-3-((Z)-2-((2-(tert-butoxy)-2-oxoethoxy)imino)-2-(2-((tert-butoxycarbonyl)amino)thiazol-4-yl)acetamido)-2-oxo-4-((2-oxooxazolidin-3-yl)methyl)azetidine-1-sulfonic acid (135 mg, 0.208 mmol), DCM (1.04 mL) and TFA (801 μl, 10.4 mmol). The crude residue purified by reverse phase prep HPLC (XSelect CSH, 19×100 mm, 5 μm, C18 column; ACN-water with 0.1% formic acid modifier, 24 mL/min), affording the title compound (25 mg, 23%) as a white powder. LCMS: Rt=0.25 min, m/z=493.0 (M+1) Method 2m_acidic; 1H NMR (500 MHz, DMSO-d6) δ 9.41 (d, J=9.1 Hz, 1H) 6.86 (s, 1H) 5.24 (dd, J=9.0, 5.8 Hz, 1H) 4.62 (s, 2H) 4.20-4.11 (m, 3H) 3.72-3.63 (m, 2H) 3.40-3.31 (m, 2H assumed; obscured by water).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174978B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-c741b1c62e9b441883fce2355ae4a3ad |
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| Source note | uspto-grants-2015_11 |
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