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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117536Generated: October 31, 2026

Benzenesulfonyl chloride → HCID 57256572, compound

https://huagongshe.com/reaction/2117536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantHCID 18376231HCID 18376231—
SolventTriethylamineHCID 8471—
ProductHCID 57256572HCID 57256572—

Reaction Steps

The title compound of Step B was prepared following the method described in Step B of Example 1 from 3-(3-{[(benzofuran-2-ylmethyl)-amino]-methyl}-phenyl)-propionic acid methyl ester of Step A and benzenesulfonyl chloride using triethylamine in place of N,N-diisopropylethylamine. 1H NMR (400 MHz, CDCl3) δ 7.83 (m, 2H), 7.52-7.42 (m, 3H), 7.26-7.09 (m, 8H), 6.39 (d, 1H), 4.46 (s, 2H), 4.39 (s, 2H), 3.68 (s, 3H), 2.88 (t, 2H), 2.57 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442702B2
Source datasetuspto-grants-2008_10
ORD IDord-e349166cce514df8aa25efcdc56df2bb
Source noteuspto-grants-2008_10