HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 135675007, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 13363602 | HCID 13363602 | — |
| Reactant | HCID 19104054 | HCID 19104054 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 135675007 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05280027 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-11bd092bc40c40aea9d1d73d3c0cd766 |
| Source note | uspto-grants-1994_01 |