HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985181Generated: October 29, 2026
Trifluoroacetic acid → HCID 9851229, compound
https://huagongshe.com/reaction/985181
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 9810099 | HCID 9810099 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 9851229 | HCID 9851229 | — |
Reaction Steps
The crude Cyanomethyl 4-{[2-(3-[(tert-Butoxy)carbonylamino]-N-{[N-({4-[(cyanomethyl)oxycarbonyl]-3-hydroxyphenyl}methyl)carbamoyl]methyl}propanoyl-amino)acetylamino]methyl}-2-hydroxybenzoate from above was dissolved in 20 mL of dichloroethane and 10 mL of trifluoroacetic acid (26.0 mmole) was added. The deprotection reaction was stirred for 2 hours at room temperature. Dichloroethane and trifluoroacetic acid were removed in vacuo. The resulting oil was dissolved in 10 mL of ethyl acetate, and the resulting solution was added dropwise to 150 mL of rapidly stirred methyl tert-butyl ether. The product precipitated over the course of one hour and was collected by filtration, washed with methyl tert-butyl ether and dried in vacuo under a high vacuum. Obtained 2.78 grams (65% for two steps) of product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06870065B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-f7fd57bda2554d33a5e7382578d315cf |
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| Source note | uspto-grants-2005_03 |
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