Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482092Generated: October 30, 2026

Diisopropylethylamine → 2-Chlorobenzene-1-sulfonic acid

https://huagongshe.com/reaction/482092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantAminoiminomethane-sulphonic acidHCID 3013981—
Reactant2-Chlorobenzenesulfonic acid 3-[(piperidin-3-yl)methoxy]-5-methylphenyl esterHCID 53655032—
SolventDimethylformamideHCID 6228—
Product2-Chlorobenzene-1-sulfonic acidHCID 1353145382.5%

Reaction Steps

A solution of 2-chlorobenzenesulfonic acid 3-[(piperidin-3-yl)methoxy]-5-methylphenyl ester (396 mg, 1.0 mmol), as prepared in the preceding step, in DMF (10 mL) containing N,N-diisopropylethylamine (0.5 mL) and aminoiminomethanesulfonic acid (248 mg, 2.0 mmol) was stirred at room temperature overnight. The DMF was removed in vacuo and the residue was purified by flash column chromatography (90:10 methylene chloride:methanol saturated with NH3) to give the title compound as a white foam (159 mg, 36%). 1H-NMR (300 MHz, CDCl3) δ 1.45-1.92 (m, 4H), 2.11 (m, 1H), 2.23 (s, 3H), 3.07 (m, 2H), 3.81 (d, 2H), 3.92 (m, 2H), 6.50 (s, 2H), 6.61 (s, 1H), 7.24 (bs, 3H), 7.40 (m, 1H), 7.63 (m, 2H), 7.95 (dd, 1H). Mass spectrum (MALDI-TOF, sinapinic acid matrix) calcd. for C20H24N3 O4SCl: 438.1 (M+H), 460.1 (M+Na), Found: 438.5, 460.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05792769
Source datasetuspto-grants-1998_08
ORD IDord-c3554de2a0044adfa27dfbcc7fab88a2
Source noteuspto-grants-1998_08