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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118135Generated: October 31, 2026

p-(Trifluoromethoxy)benzenesulphonyl chloride → HCID 11181126, compound

https://huagongshe.com/reaction/2118135

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-(Trifluoromethoxy)benzenesulphonyl chlorideHCID 523102—
ReactantHCID 69229653HCID 69229653—
ProductHCID 11181126HCID 11181126—

Reaction Steps

The title compound was prepared from ethyl 5-amino-1-benzyl-3-(4-tert-butylphenyl)-1H-indole-2-carboxylate and 4-trifluoromethoxy-benzenesulfonyl chloride followed the procedure of Example 1 Step 3 as a slight colored solid: 1H NMR (DMSO-d6) δ 1.34 (s, 9H, 5.76 (s, 2H, 7.00 (d, J=1.9 Hz, 1H, 7.07 (d, J=7.8 Hz, 4H, 7.15-7.35 (m, 5H), 7.42 (d, J=8.5 Hz, 2H, 7.54 (d, J=8.8 Hz, 2H, 7.75 (d, J=8.9 Hz, 2H, 9.95 (s, 1H, 12.50 (br s, 1H; MS (ESI) m/z 623 (MH+); MS (ESI) m/z 621 [M-H]−; HRMS calcd for C33H30F3N2O5S: 623.1825; found (ESI+): 623.1813; Anal. calcd for C33H29F3N2O5S.0.25H2O: C, 63.20; H, 4.74; N, 4.47. Found: C, 63.15; H, 4.58; N, 4.58.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442805B2
Source datasetuspto-grants-2008_10
ORD IDord-6f5ebba2e141466390c23679999bad00
Source noteuspto-grants-2008_10