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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589772Generated: October 30, 2026

Isopropanol → Isopropyl 3-{[(5-chloro-3-methyl-1-benzothien-2-yl)sulfonyl]amino}benzoate

https://huagongshe.com/reaction/589772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactant3-{[(5-Chloro-3-methyl-1-benzothien-2-yl)sulfonyl]amino}benzoic acidHCID 56941306—
ProductIsopropyl 3-{[(5-chloro-3-methyl-1-benzothien-2-yl)sulfonyl]amino}benzoateHCID 6679984357%

Reaction Steps

The product was prepared from 3-{[(5-chloro-3-methyl-1-benzothien-2-yl)sulfonyl]amino}benzoic acid (21 mg, 0.055 mmol) (Intermediate 19) and isopropyl alcohol (6.0 mg, 0.100 mmol) according to the General Procedure 7, described in Example 107, using a slightly modified reaction time (2 days). The title compound was obtained in 57% yield (13.3 mg). 1H NMR (500 MHz, CDCl3) δ ppm 1.30 (d, J=6.32 Hz, 6 H) 2.45 (s, 3 H) 5.18 (spt, J=6.32 Hz, 1 H) 6.89 (s, 1 H) 7.35 (dd, J=8.06, 7.65 Hz, 1 H) 7.41 (ddd, J=8.06, 2.35, 1.18 Hz, 1 H) 7.44 (dd, J=8.73, 1.94 Hz, 1 H) 7.68 (dd, J=2.35, 1.50 Hz, 1 H) 7.71 (dd, J=8.73, 0.61 Hz, 1 H) 7.71 (dd, J=1.94, 0.61 Hz, 1 H) 7.83 (ddd, J=7.65, 1.50, 1.18 Hz, 1 H). MS (ESI+) m/z 424 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233946B2
Source datasetuspto-grants-2016_01
ORD IDord-7f71d4e164d549128ff3e6e3dbde5b91
Source noteuspto-grants-2016_01