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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689499Generated: October 31, 2026

HCID 57989169, compound → HCID 57989183, compound

https://huagongshe.com/reaction/1689499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57989169HCID 57989169—
SolventAmmoniaHCID 222—
ProductHCID 57989183HCID 57989183—

Reaction Steps

A solution of (R)-tert-butyl 3-fluoro-5-((4-(2,2,2-trifluoroacetyl)-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)methyl)phenethyl(2-hydroxy-2-(4-hydroxy-2-oxo-2,3-dihydrobenzo[d]thiazol-7-yl)ethyl)carbamate (examples 116-182, step a) (0.7 g) in 35% aqueous ammonia solution (15 mL) was allowed to stand at 20° C. for 40 minutes. The reaction mixture was evaporated to half the initial volume under reduced pressure. Water (10 mL) was added and this solution was passed through a 10 g C18 silica cartridge which had been pre-wetted with water. The column was flushed with water (20 mL). The column was then flushed with methanol (50 mL) to bring off the product. The solvent was evaporated under reduced pressure and the residue was azeotroped with acetonitrile (×2) to afford the subtitled compound. Yield 0.580 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-38a819c01a814f1ea07451ac9076ea76
Source noteuspto-grants-2012_04