Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354216Generated: November 2, 2026

Boron tribromide → HCID 66918915, compound

https://huagongshe.com/reaction/2354216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 66919034HCID 66919034—
SolventDichloromethaneHCID 6344—
ProductHCID 66918915HCID 66918915—

Reaction Steps

Using an analogous procedure to that described in paragraph (A) in the portion of Example 24 which is concerned with the preparation of starting material, 2-amino-3-methoxybenzoic acid was reacted with 3-amino-N-cyclopropyl-4-methylbenzamide to give N-cyclopropyl-3-(8-methoxy-4-oxoquinazolin-3(4H)-yl)-4-methylbenzamide (AZ12304507); NMR Spectrum: (DMSOd6) 0.55 (m, 2H), 0.68 (m, 2H), 2.12 (s, 3H), 2.84 (m, 1H), 3.94 (s, 3H), 7.49 (m, 3H), 7.74 (d, 1H), 7.83 (s, 1H), 7.89 (d, 1H), 8.24 (s, 1H), 8.44 (s, 1H); Mass Spectrum: M+H+ 350. B) Using an analogous procedure to that described in paragraph (B) in the portion of Example 24 which is concerned with the preparation of starting material, N-cyclopropyl-3-(8-methoxy-4-oxoquinazolin-3(4H)-yl)-4-methylbenzamide was reacted with a 1M solution of boron tribromide in methylene chloride to give N-cyclopropyl-3-(8-hydroxy-4-oxoquinazolin-3(4H)-yl)-4-methylbenzamide; Mass Spectrum: M+H+ 336.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750154B2
Source datasetuspto-grants-2010_07
ORD IDord-119213d0dc5c4678a13e0aa1314689e7
Source noteuspto-grants-2010_07