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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409960Generated: October 25, 2026

Isopropyl isocyanate → tert-Butyl (2-(7-(2-fluoro-4-(3-isopropylureido)phenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)carbamate

https://huagongshe.com/reaction/409960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl isocyanateHCID 61277—
ReactantEthyl acetate hexaneHCID 21226206—
Reactanttert-Butyl (2-(7-(4-amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)carbamateHCID 57919490—
SolventEthylacetate methanolHCID 21584119—
Producttert-Butyl (2-(7-(2-fluoro-4-(3-isopropylureido)phenoxy)thieno[3,2-b]pyridin-2-yl)-1-methyl-1H-imidazol-5-yl)methyl(2-methoxyethyl)carbamateHCID 6704835664.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

The reaction mixture of aniline 46 (200 mg, 0.379 mmol) and 2-isocyanatopropane (64.5 mg, 0.758 mmol) was heated to 100° C. for 15 min in a microwave reactor. The reaction mixture was loaded directly into Biotage (Silicycle, HR, 12 g column, 50-100% EA/Hexane, then MeOH/EA, 0-20%). The collected fractions afforded the desired product 314 (150 mg, 0.245 mmol, 64.6% yield) as a white solid. MS: 613(MH)+, very weak signal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759522B2
Source datasetuspto-grants-2014_06
ORD IDord-f19158266dc1440f8e4fa56fbafa2a3c
Source noteuspto-grants-2014_06