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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743485Generated: October 30, 2026

Potassium Bromide → HCID 9853529, compound

https://huagongshe.com/reaction/1743485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
ReactantHCID 86583666HCID 86583666—
ProductHCID 9853529HCID 9853529—

Reaction Steps

The title compound was prepared as a light green solid (0.073 g, 62%) from 4-{2-[3,3″-Dichloro-5′-(8-indol-1-yl-octylcarbamoyl)-[1,1′:3′,1″]terphenyl-2′-yloxy]-ethoxy}benzoic acid, methyl ester using a procedure similar to step 4 of example 165; dec. >65° C.; 1H NMR (400 MHz, DMSO-d6) δ 1.16–1.30 (m, 8H), 1.44–1.53 (m, 2H), 1.67–1.76 (m, 2H), 3.20–3.26 (m, 2H), 3.56–3.60 (m, 2H), 3.72–3.76 (m, 2H), 4.12 (t, J=7.0 Hz, 2H), 6.37 (dd, J=0.66, 3.1 Hz, 1H), 6.66–6.70 (m, 2H), 6.94–6.99 (m, 1H), 7.06–7.10 (m, 1H), 7.32 (d, J=3.1 Hz, 1H), 7.38–7.52 (m, 6H), 7.57–7.60 (m, 2H), 7.67 (t, J=1.8 Hz, 2H), 7.76–7.80 (m, 2H), 7.88 (s, 2H), 8.55 (t, J=5.7 Hz, 1H), 12.54 (broad s, 1H); IR (KBr) 3420, 2920, 1680, 1600, 1260, 1160 cm−1; mass spectrum [(−)APCI], m/z 747 (M−H)−; Anal. Calcd. for C44H42Cl2N2O5: C, 70.49; H, 5.65; N, 3.74. Found: C, 70.12; H, 6.01; N, 3.44.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07008636B2
Source datasetuspto-grants-2006_03
ORD IDord-170c5962134c41c88ba2e8cf653bba83
Source noteuspto-grants-2006_03