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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915347Generated: October 30, 2026

1,1'-Biphenyl, 4-(bromomethyl)- → Ethyl 1-(1,1'-biphenyl-4-ylmethyl)-5-nitro-3-phenyl-1H-indole-2-carboxylate

https://huagongshe.com/reaction/915347

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-Biphenyl, 4-(bromomethyl)-HCID 257716—
Reactantethyl 5-nitro-3-phenyl-1H-indole-2-carboxylateHCID 741309—
ProductEthyl 1-(1,1'-biphenyl-4-ylmethyl)-5-nitro-3-phenyl-1H-indole-2-carboxylateHCID 69228457—

Reaction Steps

Ethyl 1-(1,1′-biphenyl-4-ylmethyl)-5-nitro-3-phenyl-1H-indole-2-carboxylate was prepared from ethyl 5-nitro-3-phenyl-1H-indole-2-carboxylate and 4-bromomethylbiphenyl according to the procedure of Example 1 Step 1 as a yellowish solid: 1H NMR (DMSO-d6) δ 0.95 (t, J=7.0 Hz, 3 H), 4.13 (q, J=7.0 Hz, 2 H), 5.96 (s, 2 H), 7.30-7.32 (m, 14 H), 7.62 (d, J=2.3 Hz, 1 H), 8.25 (d, J=2.8 Hz, 1 H), 8.36 (s, 1 H); MS (ESI) m.z 477 (MH+); HRMS calcd for C30H25N2O4: 477.1815; found (ESI+): 477.1806; Anal. calcd for C30H24N2O4: C, 75.62; H, 5.08; N, 5.88. Found: C, 75.25; H, 5.18; N, 5.47.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265148B2
Source datasetuspto-grants-2007_09
ORD IDord-c1f049a441f34e338ed0076137800fc6
Source noteuspto-grants-2007_09