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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583984Generated: November 1, 2026

Trifluoroacetic acid → HCID 53789842, compound

https://huagongshe.com/reaction/1583984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl alpha-oxobenzenebutanoateHCID 562087—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 13605255HCID 13605255—
ReactantAcetic Acid Mixture with Hydrobromic AcidHCID 21893785—
ProductHCID 53789842HCID 53789842—

Reaction Steps

N-[N5 -(N-Cbz-glycyl)-L-ornithyl]-L-proline was prepared as described in Example 4. The reductive alkylation of TFA salt (132 mg, 0.314 mmol) with ethyl 2-oxo-4-phenylbutyrate (324 mg, 1.57 mmol) and sodium cyanoborohydride (59.2 mg, 0.942 mmol) was carried out in the usual manner. The work up, including 30-32% HBr/HOAc treatment, was the same as that described in Example 1. Both ms and nmr were consistent with the structure for N-[N2 -(1-ethoxycarbonyl-3-phenylpropyl)-N5 -glycyl-L-ornithyl]-L-proline (47.5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04555502
Source datasetuspto-grants-1985_11
ORD IDord-c1955ce8ada94351b1d4180a47354b99
Source noteuspto-grants-1985_11