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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864260Generated: October 31, 2026

Picolyl chloride hydrochloride → HCID 57974302, compound

https://huagongshe.com/reaction/1864260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolyl chloride hydrochlorideHCID 23392—
ReactantHCID 69058281HCID 69058281—
ProductHCID 57974302HCID 5797430234%

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]-N-methylacetamide to give the title compound in 34% yield; NMR spectrum (DMSO-d6, 373K) 1.20 (d, 3H), 1.85 (s, 3H), 2.80 (s, 3H), 3.00 (m, 1H), 4.30 (m, 1H), 4.40 (m, 1H), 5.30 (s, 2H), 7.20 (m, 2H), 7.40 (m, 2H), 7.50 (d, 1H), 7.60 (d, 1H), 7.70 (t, 1H), 7.80 (m, 1H), 7.90 (d, 1H), 8.40 (s, 1H), 8.60 (d, 1H), 9.60 (s, 1H); Mass spectrum MH+ 492.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625908B2
Source datasetuspto-grants-2009_12
ORD IDord-412b39bba62e41c0b334fcd2c4468b88
Source noteuspto-grants-2009_12