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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227254Generated: October 30, 2026

Carbon Tetrachloride → 4-(6-Chloro-2,3-dihydro-indol-1-yl)-6-methyl-pyrido[3,4-d]pyrimidine

https://huagongshe.com/reaction/2227254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantTriphenylphosphineHCID 11776—
Reactant6-Chloro-2,3-dihydro-1h-indoleHCID 258567—
Reactant6Methyl-pyrido[3,4-d]pyrimid-4oneHCID 135992001—
Solvent1,2-DichloroethaneHCID 11—
Product4-(6-Chloro-2,3-dihydro-indol-1-yl)-6-methyl-pyrido[3,4-d]pyrimidineHCID 1847328830%

Reaction Conditions

Temperature60 °C

Reaction Steps

6Methyl-pyrido[3,4-d]pyrimid-4one (200 mg, 1.24 mmol), polymer-supported triphenylphosphine (2.06 g of 3.0 mmol Pig resin, 6.20 mmol) and anhydrous carbon tetrachloride (1.20 mL, 12.40 mmol) were combined in 1,2-dichloroethane (6 mL). The mixture was heated to 60° C. under an atmosphere of dry N2(g) for 18 hours. 6-Chloroindoline (1.1 eq.) was added and heating was continued at 60° C. for another 18 hours. The triphenyphosphine-bearing resin was filtered off and washed several times with chloroform. The filtrate and washings were concentrated in vacuo and preparative reversed-phase (C18) chromatography utilizing a gradient of 15% to 70% MeCN/pH4.5, 50 mM NH4OAc followed by lyophilization of the appropriate fractions afforded the title product (30%) as its free-base: MP: 232-234° C.; LC-MS: 297 (MH+); anal. RP-HPLC: 4.33 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413971B1
Source datasetuspto-grants-2002_07
ORD IDord-38fd3f8d32b64abc890c32277956bf7b
Source noteuspto-grants-2002_07