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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864264Generated: October 30, 2026

Picolyl chloride hydrochloride → HCID 57974281, compound

https://huagongshe.com/reaction/1864264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolyl chloride hydrochlorideHCID 23392—
ReactantHCID 69057304HCID 69057304—
ProductHCID 57974281HCID 5797428157%

Reaction Steps

The procedure described in Example 3 was repeated using picolyl chloride hydrochloride and N-[(1S)-2-({4-[(3-chloro-4-hydroxyphenyl)amino]quinazolin-5-yl}oxy)-1-methylethyl]-2-hydroxyacetamide to give the title compound in 57% yield; NMR spectrum (DMSO-d6) 1.23 (d, 3H), 3.64-3.81 (m, 2H), 4.24-4.36 (m, 2H), 4.45-4.59 (m, 1H), 5.29 (s, 2H), 5.45 (t, 1H), 7.13-7.23 (m, 2H), 7.35 (t, 2H), 7.49-7.53 (m, 1H), 7.56-7.59 (m, 1H), 7.72 (t, 1H), 7.87 (t, 1H), 7.99-8.02 (m, 2H), 8.46 (s, 1H), 8.59 (d, 1H), 9.75 (s, 1H); Mass spectrum MH+ 493.95.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625908B2
Source datasetuspto-grants-2009_12
ORD IDord-f65870f84d7e446398ca63558d180b58
Source noteuspto-grants-2009_12