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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864347Generated: October 31, 2026

Dichloromethane → HCID 57974285, compound

https://huagongshe.com/reaction/1864347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantMethyl IsocyanateHCID 12228—
ReactantN-[3-chloro-4-(pyridin-2-ylmethoxy)phenyl]-5-[2-(methylamino)ethoxy]quinazolin-4-amineHCID 69065361—
ProductHCID 57974285HCID 5797428583%

Reaction Steps

Methyl isocyanate (0.035 ml) was added slowly to a stirred solution of N-[3-chloro-4-(pyridin-2-ylmethoxy)phenyl]-5-[2-(methylamino)ethoxy]quinazolin-4-amine (obtained as described in Example 1, preparation of starting materials, 217 mg) in DCM (10 ml). The resulting solution was stirred for 2 hours and then evaporated. The residue was triturated with acetonitrile and the resulting solid washed with ether to give the title compound as a solid (205 mg, 83%); NMR spectrum (DMSO-d6 @ 373K) 2.85 (s, 3H), 2.95 (s, 3H), 3.75-3.85 (t, 2H), 4.35-4.45 (t, 2H), 5.25 (s, 2H), 5.90-6.00 (bs, 1H), 7.10-7.15 (d, 1H), 7.15-7.25 (d, 1H), 7.30-7.37 (t, 2H), 7.52-7.60 (m, 2H), 7.65-7.73 (t, 1H), 7.80-7.86 (m, 1H), 7.94-7.99 (d, 1H), 8.44 (s, 1,H), 8.55-8.60 (d, 1H), 9.80 (s, 1H); Mass spectrum MH+ 493.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625908B2
Source datasetuspto-grants-2009_12
ORD IDord-e22f46a1c4fa4d69b94ade261ee9d5b5
Source noteuspto-grants-2009_12