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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413728Generated: October 30, 2026

Trifluoroacetic acid → HCID 12969041, compound

https://huagongshe.com/reaction/413728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86584667HCID 86584667—
ProductHCID 12969041HCID 1296904158%

Reaction Steps

This compound was prepared from tert-butyl (2S)-3-[4-(benzyloxy)phenoxy]-2-hydroxypropyl{4-[(2,4-dioxo-1,3-thiazolidin-5-yl)amino]phenethyl}carbamate and trifluoroacetic acid in substantially the same manner as described in example 1, step e, with one modification, the product was isolated as the free base and recrystallized from methanol, tetrahydrofuran, hexanes to give a yellow foam solid (58% yield): mp 152° C.; MS m/e 508 (M+H)+; 1H NMR (DMSO-d6 300 MHz) δ2.68 (m, 2H), 2.81 (m, 1H), 2.88 (m, 4H), 3.85 (m, 2H), 4.00 (m, 1H), 5.02 (s, 2H), 5.45 (br, 1H), 5.99 (d, 1H), 6.59 (d, 2H), 6.66 (d, 1H), 6.84 (d, 2H), 6.86 (m, 2H) 6.92 (m, 2H), 7.28 (m, 5H), 8.80 (br, 1 H);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06569873B2
Source datasetuspto-grants-2003_05
ORD IDord-73be69e358544b269c0ed953a20e93bc
Source noteuspto-grants-2003_05