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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265250Generated: October 31, 2026

4-Chloro-2-(quinoxaline-5-sulfonylamino)benzoic acid → HCID 11657139, compound

https://huagongshe.com/reaction/2265250

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-(quinoxaline-5-sulfonylamino)benzoic acidHCID 16090778—
ReactantHCID 68769668HCID 68769668—
ProductHCID 11657139HCID 11657139—

Reaction Steps

3-Benzo[b]thiophen-3-yl-2-(tert-butoxycarbonylamino)-propionic acid was treated as in EXAMPLE 2, Part A, to produce (S)-2-amino-3-benzo[b]thiophen-3-yl-propionic acid methyl ester hydrochloride as a white solid. This ester was coupled to 4-chloro-2-(quinoxaline-5-sulfonylamino)-benzoic acid as in EXAMPLE 1, Part C, to afford the title compound. HPLC: RT=10.33 min. MS (ESI−): mass calcd. for C27H21ClN4O5S2, 580.06; m/z found, 579/581 [M−H]−. 1H NMR (400 MHz, CDCl3): 11.35 (s, 1H), 8.94 (d, J=1.8, 1H), 8.85 (d, J=1.8, 1H), 8.58 (dd, J=7.3, 1.4, 1H), 8.31 (dd, J=8.5, 1.3, 1H), 7.90-7.86 (m, 2H), 7.77 (d, J=2.0, 1H), 7.72-7.70 (m, 1H), 7.37-7.26 (m, 2H), 7.09 (s, 1H), 7.00 (d, J=8.4, 1H), 6.83 (dd, J=8.4, 2.0, 1H), 6.45 (d, J=7.1, 1H), 5.09-5.05 (m, 1H), 3.77 (s, 3H), 3.53 (dd, J=14.7, 5.8, 1H), 3.45 (dd, J=14.8, 5.2, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855292B2
Source datasetuspto-grants-2010_12
ORD IDord-42a34d4b48764dde8d5dfc6ba00d01b2
Source noteuspto-grants-2010_12