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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118116Generated: October 31, 2026

8-Quinolinesulfonyl chloride → HCID 11410040, compound

https://huagongshe.com/reaction/2118116

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Quinolinesulfonyl chlorideHCID 29220—
Reactantethyl 5-amino-1-benzyl-3-phenyl-1H-indole-2-carboxylateHCID 69229300—
ProductHCID 11410040HCID 11410040—

Reaction Steps

The title compound was prepared from ethyl 5-amino-1-benzyl-3-phenyl-1H-indole-2-carboxylate and quinoline-8-sulfonyl chloride followed the procedure of Example 1 Step 3 as a pale yellow solid: 1H NMR (DMSO-d6) δ 5.66 (s, 2H, 6.90 (d, J=2.0 Hz, 1H, 6,95-7.05 (m, 5H, 7.15-7.28 (m, 3H, 7.30-7.45 (m, 4H, 7.64 (t, J=7.8 Hz, 1H, 7.75 (dd, J=8.3, 4.1 Hz, 1H, 8.17 (dd, J=7.3, 1.3 Hz, 1H, 8.27 (dd, J=8.2, 1.2 Hz, 1H, 8.57 (dd, J=8.3, 1.7 Hz, 1H, 9.12 (dd, J=4.2, 1.6 Hz, 1H, 9.67 (s, 1H, 12.97 (br s, 1H; MS (ESI) m/z 534 (MH+); MS (ESI) m/z 532 [M-H]−; HRMS calcd for C31H24N3O4S: 534.1477; found (ESI+): 534.1481; Anal. calcd for C31H23N3O4S.0.25H2O: C, 69.19; H, 4.40; N, 7.81. Found: C, 69.28; H, 4.31; N, 7.73.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442805B2
Source datasetuspto-grants-2008_10
ORD IDord-e2580609ee8f4f05850e19a067d022be
Source noteuspto-grants-2008_10