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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867729Generated: October 31, 2026

Formaldehyde → HCID 57979806, compound

https://huagongshe.com/reaction/1867729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant4-Amino-1-(tert-butoxycarbonyl)piperidine-4-carboxylic acidHCID 693797—
Reactant4-[(3-Chloro-2-fluorophenyl)amino]-7-methoxyquinazoline-6-carbaldehydeHCID 11573492—
Reactant3-Amino-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acidHCID 24730316—
ProductHCID 57979806HCID 57979806—

Reaction Steps

4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazoline-6-carbaldehyde was coupled with 3-amino-1-(tert-butoxycarbonyl)pyrrolidine-3-carboxylic acid (commercially available or may be prepared made using analogous methodology as that described for the preparation of 4-amino-1-(tert-butoxycarbonyl)piperidine-4-carboxylic acid in J. Org. Chem. 1996, 61, 7650-7651). The resultant product was deprotected and methylated by reaction with aqueous formaldehyde using analogous methods to those described for the equivalent steps in Example 68 to give 3-[({4-[(3-chloro-2-fluorophenyl)amino]-7-methoxyquinazolin-6-yl}methyl)(methyl)amino]-1-methylpyrrolidine-3-carboxylic acid as a pale yellow foam; Mass Spectrum: (M+H)+ 474.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632840B2
Source datasetuspto-grants-2009_12
ORD IDord-a7144fa7b28c43c0b027b76b5adb3f43
Source noteuspto-grants-2009_12