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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394086Generated: October 29, 2026

HCID 22647914, compound → HCID 22648046, compound

https://huagongshe.com/reaction/394086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22647914HCID 22647914—
ReactantHCID 22647964HCID 22647964—
ReactantHCID 22648046HCID 22648046—
ReactantHCID 22648076HCID 22648076—
ProductHCID 22648046HCID 22648046—
ProductHCID 22648069HCID 22648069—

Reaction Steps

The title compound was prepared from 1-(2,6-dichlorophenyl)-3-methyl-5-(2-chloro-4-fluorophenyl)-7-trifluoromethylsulfonato-3,4-dihydro-2(1H)-quinazolinone as described in EXAMPLE 41. 1-(2,6-dichlorophenyl)-3-methyl-5-(2-chloro-4-fluorophenyl)-7-trifluoromethylsulfonato-3,4-dihydro-2(1H)-quinazolinone was prepared from 1-(2,6-dichlorophenyl)-3-methyl-5-(2-chloro-4-fluorophenyl)-7-methoxy-3,4-dihydro-2(1H)-quinazolinone (INTERMEDIATE 58) as described in INTERMEDIATE 48 and INTERMEDIATE 60. 1H NMR(CDCl3, 500 MHz): diastereomeric atropisomers δ 1.32 (m, 3H), 2.37 (brs, 2H), 2.51 (brm, 1H), 3.10 (t, 2H, J=5.7 Hz), 3.53 (brs, 2H), 4.36 (m, 0.5H), 4.47 (m, 0.5H), 5.51 (d, 0.5H, 2.9 Hz), 5.58 (d, 0.5H, J=2.7 Hz), 5.90 (brs, 1H), 6.13 (s, 0.5H), 6.15 (s, 0.5H), 6.83 (s, 0.5H), 6.90 (s, 0.5H), 7.09-7.13 (m, 1H), 7.28-7.42 (m, 3H), 7.51-7.58 (m, 2H). MS(ES) 516 (M+H); LC 1: 2.22 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809199B2
Source datasetuspto-grants-2004_10
ORD IDord-60e446644bbb4b4c8d965268782ef3d4
Source noteuspto-grants-2004_10