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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475490Generated: October 29, 2026

Dimethylformamide → Propyl {(7R)-7-{[(4-fluorophenyl)sulfonyl](methyl)amino}-6,7,8,9-tetrahydro-pyrido[1,2-alpha]indol-10-yl}acetate

https://huagongshe.com/reaction/475490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
ReactantPropyl (7R)-7-[[(4-fluorophenyl)sulfonyl]amino]-6,7,8,9-tetrahydropyrido[1,2-a]indole-10-acetateHCID 58399163—
SolventAmmonium ChlorideHCID 25517—
ProductPropyl {(7R)-7-{[(4-fluorophenyl)sulfonyl](methyl)amino}-6,7,8,9-tetrahydro-pyrido[1,2-alpha]indol-10-yl}acetateHCID 5839916698%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (1.05 equiv.) was added to a 0° C. DMF solution (0.14 M) of propyl {(7R)-7-{[(4-fluorophenyl)sulfonyl]amino}-6,7,8,9-tetrahydropyrido [1,2-α]indol-10-yl }acetate from Step 7 and the mixture was stirred at 0 ° C. for 30 min. lodomethane (3 equiv.) was added and the reaction was stirred at 0° C. for 2 h. The mixture was poured in aqueous NH4Cl and extracted with Et2O (2×). The combined organic extracts were washed with water (3×), brine and then dried with MgSO4, filtered and concentrated under vacuum. The residue was purified by column chromatography on silica gel using a CombiFlashRF (Teledyne ISCO) eluting with EtOAc/Hex (5:95 to 50:50) to give the title compound (98%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637541B2
Source datasetuspto-grants-2014_01
ORD IDord-df32f4b15e954c2f8c007c261b8dcce2
Source noteuspto-grants-2014_01