HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680592Generated: October 30, 2026
Trifluoroacetic acid → HCID 70567604, compound
https://huagongshe.com/reaction/1680592
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 70565002 | HCID 70565002 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70567604 | HCID 70567604 | — |
Reaction Steps
To a solution of 1.862 g of methyl Boc-L-phenylalanyl-2-amino-1-adamantanecarboxylate (Isomer A) in 10 ml of methylene chloride is added 5 ml of trifluoracetic acid. After 15 minutes at room temperature the reaction mixture is concentrated to a small volume and 5 ml of cold potassium carbonate is added. The mixture is extracted twice with 20 ml of chloroform. The combined chloroform extracts are dried over sodium sulfate to give methyl L-phenylalanyl-2-amino-1-adamantanecarboxylate (Isomer A) as a crystalline solid melting at 160°-167° C. Under a nitrogen atmosphere at -50° C. a dry (1 g of 4 A sieves) solution of 1.878 g of Boc-L-tyrosyl-D-methionyl-glycine and 0.444 ml of N-methylmorpholine in 25 ml of tetrahydrofuran is stirred while 0.52 ml of isobutylchloroformate is added. The reaction mixture is allowed to warm to -10° C. for 10 minutes then cooled to -40° C. and 1.24 g of methyl L-phenylalanyl- 2-amino-1-adamantanecarboxylate is added. The reaction mixture is stirred overnight at room temperature. Upon the addition of water a solid separates and is collected by filtration, washed and dried. The residue is dissolved in methanol, filtered through Filter Cel, concentrated and diluted with equal volumes of ethyl acetate and ether. The solid which precipitates is collected by filtration, washed with ether and dried to give methyl Boc-L-tyrosyl-D-methionyl-glycyl-L-phenylalanyl-2-amino-1-adamantanecarboxylate (Isomer A). 2.34 Grams of this compound is dissolved in 10 ml of acetic acid and 20 ml of a 5 N solution of hydrogen chloride in dioxane is added. The reaction mixture is concentrated under a stream of nitrogen for 11/2 hours and diluted with 150 ml of ether. The solid which forms is collected, dissolved in methanol, concentrated to about 10 ml and diluted with 40 ml of water then allowed to stand overnight at room temperature. The solution is filtered and lyophilized to give methyl L-tyrosyl-D-methionyl-glycyl-L-phenylalanyl-2-amino-1-adamantanecarboxylate hydrochloride (Isomer A) which is represented by the following formula ##STR47##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04273704 |
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| Source dataset | uspto-grants-1981_06 |
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| ORD ID | ord-9d653b7b962a437a8f5832c11db58bb2 |
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| Source note | uspto-grants-1981_06 |
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