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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278774Generated: November 2, 2026

Trifluoroacetic acid → HCID 10283272, compound

https://huagongshe.com/reaction/1278774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 10305737HCID 10305737—
SolventWaterHCID 962—
ProductHCID 10283272HCID 10283272—

Reaction Steps

This compound was prepared from tert-butyl 2-{(2,5-difluorobenzyl)[(4-{4-[((2R)-2-hydroxy-2-{4-hydroxy-3-[(methylsulfonyl)amino]phenyl}ethyl)amino]-1-piperidinyl}phenyl)sulfonyl]amino}acetate in substantially the same manner, as described in Example 53, with one change; the mixture was stirred at room temperature for 20 hours. The volatiles were removed and the product was purified by reverse phase chromatography to give a white solid (1.44 9, 42% yield): mp 80-82° C.; MS m/e 669 (M+H)+; 1H NMR (DMSO-d6 400 MHz) 81.62 (m, 2H), 2.11 (m, 2H), 2.85 (m, 2H), 2.94 (s, 3H), 2.96 (m, 1H), 3.11 (m, 1H), 3.34 (m, 1H), 3.88 (s, 2H), 3.99 (m, 2H), 4.37 (s, 2H), 4.79 (m, 1H), 6.01 (br, 1H), 6.90 (d, 1H), 7.05 (m, 3H), 7.18 (m, 3H), 7.21 (s, 1H), 7.59 (d, 2H), 8.58 (brs, 1H), 8.66 (brs, 1H), 8.74 (brs, 1H), 10.01 (brs, 1H); Analysis for C29H34F2N4O8S2×2.0 CF3COOH×0.73 H2O Calc'd: C, 43.52; H, 4.11 ; N, 6.15 Found: C, 42.95; H, 3.93; N, 6.08.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06444685B1
Source datasetuspto-grants-2002_09
ORD IDord-45a89b3fd082497195c3438456f36fc5
Source noteuspto-grants-2002_09