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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2038085Generated: October 30, 2026

Dimethylformamide → HCID 59129228, compound

https://huagongshe.com/reaction/2038085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium AzideHCID 33557—
ReactantHCID 86615739HCID 86615739—
ProductHCID 59129228HCID 59129228—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution (R)-3-(2-tert-butyl-5-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-1H-indol-1-yl)-2-hydroxypropyl-4-methylbenzenesulfonate (3.2 g, 5.0 mmol) in DMF (6 mL) was added sodium azide (2.0 g, 30 mmol). The reaction was heated at 80° C. for 2 h. The mixture was partitioned between 20 mL ethyl acetate and 20 mL water. The layers were separated and the organic layer was evaporated. The residue was purified using column chromatography (0-85% ethyl acetate/hexane) to give (R)- N-(1-(3-azido-2-hydroxypropyl)-2-tert-butyl-1H-indol-5-yl)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-cyclopropanecarboxamide (2.48 g). LC/MS (M+1)=512.5. 1 H NMR (400 MHz, CDCl3) δ 7.55(d, 1H, J=2 Hz), 7.31(m, 3H), 6.96(s, 1H), 6.94(dd, 1H, J=2, 8 Hz), 6.22(s, 1H), 4.33 (m, 1H), 4.31(dd, 1H, J=6, 15 Hz), 4.28(dd, 1H, J=11, 15 Hz), 4.18(m, 1H), 3.40(dd, 1H, J=3, 6 Hz), 3.36(dd, 1H, J=3, 6 Hz), 2.40(br s, 1H), 1.74(m, 2H), 1.40(s, 9H), 1.11(m, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575209B2
Source datasetuspto-grants-2013_11
ORD IDord-3617133fea0243a9a731921a2447214a
Source noteuspto-grants-2013_11