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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013091Generated: October 30, 2026

Hexane → HCID 44243040, compound

https://huagongshe.com/reaction/1013091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantHCID 16708834HCID 16708834—
ReactantHCID 44243038HCID 44243038—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
ProductHCID 44243040HCID 4424304020%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 2.0 M hexane solution of (diethylamino)dimethylaluminum (3.2 equivalents) in dry benzene (0.26 M) was cooled to −15° C., a solution of ethyl 3-(8-(2-(3-ethylureido)benzo[b]thiophene-3-carbonyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-en-2-yl)propanoate (10 (Example 10), 12 mg, 1.0 equivalent) in THF (0.16M) was added; the mixture was heated to 80° C. for 6 hrs. The mixture was cooled in an ice bath; then a saturated aqueous Rochelle's solution was added and stirred for 1 hr, then partitioned between ethyl acetate and water and the separated organics was washed with brine and dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by preparatory LCMS to afford N,N-diethyl-3-(8-(2-(3-ethylureido)benzo[b]thiophene-3-carbonyl)-4-oxo-1,3,8-triazaspiro[4.5]dec-1-en-2-yl)propanamide (10, 20%). Two rotamers observed (ratio 1.3:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981904B2
Source datasetuspto-grants-2011_07
ORD IDord-1d3b65ccb6564805a438ed9d193f40e5
Source noteuspto-grants-2011_07