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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864267Generated: November 1, 2026

Picolyl chloride hydrochloride → HCID 69062149, compound

https://huagongshe.com/reaction/1864267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolyl chloride hydrochlorideHCID 23392—
ReactantHCID 69059716HCID 69059716—
ProductHCID 69062149HCID 6906214963%

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]acetamide to give the title compound in 63% yield; NMR spectrum (DMSO-d6) 1.21 (s, 3H), 1.73 (s, 3H), 4.12-4.30 (m, 2H), 4.33-4.43 (m, 1H), 5.29 (s, 2H), 7.15-7.25 (m, 2H), 7.35 (t, 2H), 7.51-7.59 (m, 2H), 7.72 (t, 1H), 7.87 (t, 1H), 7.99 (s, 1H), 8.14 (d, 1H), 8.48 (s, 1H), 8.59 (d, 1H), 9.80 (s, 1H); Mass spectrum MH+ 478.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625908B2
Source datasetuspto-grants-2009_12
ORD IDord-7b3a047f6e6e4c25a1d449fff4c16c51
Source noteuspto-grants-2009_12