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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351966Generated: October 29, 2026

1-[(2-methyl-5,8-dihydro-4-quinolinyl)methyl]-1H-indole-5-carbonyl chloride → 1-tert-butyl 3-methyl 4-[({1-[(2-methyl-4-quinolinyl)methyl]-1H-indol-5-yl}carbonyl)amino]-1,3-pyrrolidinedicarboxylate

https://huagongshe.com/reaction/351966

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[(2-methyl-5,8-dihydro-4-quinolinyl)methyl]-1H-indole-5-carbonyl chlorideHCID 22258380—
Reactant1-tert-Butyl 3-methyl 4-aminopyrrolidine-1,3-dicarboxylateHCID 23590635—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-tert-butyl 3-methyl 4-[({1-[(2-methyl-4-quinolinyl)methyl]-1H-indol-5-yl}carbonyl)amino]-1,3-pyrrolidinedicarboxylateHCID 2225849770%

Reaction Steps

The 1-tert-butyl 3-methyl 4-amino-1,3-pyrrolidinedicarboxylate (0.10 g, 0.41 mmol) was combined with the acid chloride from step (501b) (0.10 g, 0.32 mmol) in methylene chloride (15 mL) and water saturated sodium bicarbonate (15 mL). The reaction was stirred for 3.5 h, partitioned between methylene chloride and water. The organic layer was washed with brine, dried over magnesium sulfate and concentrated to give a solid. This was purified by flash chromatography on silica gel eluting hexane: ethyl acetate (30:60, v:v) to give the 1-tert-butyl 3-methyl 4-[({1-[(2-methyl-4-quinolinyl)methyl]-1H-indol-5-yl}carbonyl)amino]-1,3-pyrrolidinedicarboxylate (0.120 g, 70%) as a solid, MS (M+H)+=543.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743807B2
Source datasetuspto-grants-2004_06
ORD IDord-2a55b1d680f6412d919ea174e43e4c21
Source noteuspto-grants-2004_06