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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991768Generated: November 1, 2026

Trifluoroacetic acid → HCID 12969041, compound

https://huagongshe.com/reaction/991768

Reaction equation

Participants

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

Reaction Steps

This compound was prepared from tert-butyl (2 S)-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, 2 H), 2.81 (m, 1 H), 2.88 (m, 4 H), 3.85 (m, 2 H), 4.00 (m, 1 H), 5.02 (s, 2 H), 5.45 (br, 1 H), 5.99 (d, 1 H), 6.59 (d, 2 H), 6.66 (d, 1 H), 6.84 (d, 2 H), 6.86 ( m, 2 H) 6.92 (m, 2 H), 7.28 (m, 5 H), 8.80 (br, 1 H);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465501B2
Source datasetuspto-grants-2002_10
ORD IDord-af4c5111badf43858bb2bfd4b3dad153
Source noteuspto-grants-2002_10