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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055103Generated: October 31, 2026

Ethyl orthoformate → HCID 53690208, compound

https://huagongshe.com/reaction/2055103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantHCID 22238210HCID 22238210—
ProductHCID 53690208HCID 5369020863%

Reaction Steps

Using an analogous procedure to that described in Example 18, N-[2-fluoro-5-(3-fluoro-5-morpholinobenzamido)phenyl]-2-amino-5-(4-methylhomopiperazin-1-yl)benzamide was reacted with triethyl orthoformate to give the title compound in 63% yield; NMR Spectrum: (DMSOd6) 1.92 (m, 2H), 2.25 (s, 3H), 2.46 (m, 2H), 2.64 (m, 2H), 3.21 (t, 4H), 3.53 (t, 2H), 3.6 (m, 2H), 3.72 (t, 4H), 6.99 (d, 1H), 7.12 (d, 1H), 7.23 (m, 1H), 7.3 (s, 1H), 7.36 (m, 1H), 7.48 (t, 1H), 7.58 (d, 1H), 7.87 (m, 1H), 7.96 (m, 1H), 8.06 (s, 1H), 10.43 (s, 1H); Mass Spectrum: M+H+ 575.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332483B2
Source datasetuspto-grants-2008_02
ORD IDord-d95de51beada4c33924d14522908ec2d
Source noteuspto-grants-2008_02