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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500702Generated: October 29, 2026

N-(3-Chloro-4-fluorophenyl)-7-methoxy-6-nitroquinazolin-4-amine → N4-(3-Chloro-4-fluorophenyl)-7-methoxy-4,6-quinazolinediamine

https://huagongshe.com/reaction/500702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-Chloro-4-fluorophenyl)-7-methoxy-6-nitroquinazolin-4-amineHCID 21847811—
CatalystNickelHCID 935—
SolventTetrahydrofuranHCID 8028—
ProductN4-(3-Chloro-4-fluorophenyl)-7-methoxy-4,6-quinazolinediamineHCID 2184782699%

Reaction Steps

7.1 g of (3-Chloro-4-fluoro-phenyl)-(7-methoxy-6-nitro-quinazolin-4-yl)-amine was reduced using Raney nickel catalyst in THF, then filtered and evaporated to give 6.4 g N4-(3-Chloro-4-fluoro-phenyl)-7-methoxy-quinazoline-4,6-diamine (99% yield). This product was reacted with 4-Chloro-but-2-enoyl chloride as described in Scheme 1 to provide 4-Chloro-but-2-enoic acid [4-(3-chloro-4-fluoro-phenylamino)-7-methoxy-quinazolin-6-yl]-amide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772243B2
Source datasetuspto-grants-2010_08
ORD IDord-6fce9690bdba4702add5b871463c9db1
Source noteuspto-grants-2010_08