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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198194Generated: November 2, 2026

Ammonia → HCID 135675007, compound

https://huagongshe.com/reaction/1198194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 13363602HCID 13363602—
ReactantHCID 19104054HCID 19104054—
SolventMethanolHCID 887—
ProductHCID 135675007HCID 135675007—

Reaction Steps

The process described in Example 1 was repeated except that (R/S)-2-amino-2-methyl-3-phenylpropiononitrile (Eur. J. Med. Chem. Clin. Ther., 1975, 10, 117) was used in place of (-)-(2R)-2-amino-2-phenylethanol and that the N-(2-cyano-1-phenylprop-2-yl)-p-[N-(2-methyl-4-oxo-3-(pivaloyloxymethyl)-3,4-dihydroquinazolin-6-ylmethyl)-N-(prop-2-ynyl)amino]benzamide so produced was dissolved in methanol which had been saturated with ammonia gas and the mixture was stirred at laboratory temperature for 24 hours. The mixture was evaporated to give N-(2-cyano-1-phenylprop-2-yl)-p-[N-(2-methyl-4-oxo-3,4-dihydroquinazolin-6-ylmethyl)-N-(prop-2-ynyl)amino]benzamide, m.p. 208°-209° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05280027
Source datasetuspto-grants-1994_01
ORD IDord-11bd092bc40c40aea9d1d73d3c0cd766
Source noteuspto-grants-1994_01