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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420296Generated: October 29, 2026

Methoxyacetyl chloride → HCID 131729374, compound

https://huagongshe.com/reaction/420296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxyacetyl chlorideHCID 96623—
ReactantHCID 131729372HCID 131729372—
ProductHCID 131729374HCID 131729374—

Reaction Steps

The title compound was prepared in analogous manner as described for example 8q and 8r from N-{4-[(3aR,7S,7aS)-3-(3-tert-butyl-benzyl)-2,5,5-trioxo-octahydro-1-oxa-5lambda*6*-thia-3-aza-inden-7-ylmethyl]-2-ethyl-6-fluoro-phenyl}-2-chloro-acetamide and methoxy-acetyl chloride to yield after preparative HPLC purification (Sunfire C18 OBD 5 μm, 100×30, 5-100% ACN in water+0.1% TFA gradient, 25 min) the title compound as a light yellow amorphous solid: TLC (EtOAc-MeOH 9:1) Rf=0.56; UPLC RtD=1.298 min; ESIMS [M+H]+=535; 1H NMR (600 MHz, DMSO-d6): δ 9.99 (s, 1H), 9.31 (s, 1H), 9.08 (s, 1H), 7.68 (s, 1H), 7.44 (dd, 1H), 7.39 (m, 3H), 6.96 (d, 1H), 6.92 (s, 1H), 6.23 (s, 1H), 4.23 (m, 4H), 4.01 (s, 2H), 3.91 (d, 1H), 3.66 (m, 2H), 3.38 (s, 3H), 3.26 (dd, 1H), 3.17 (m, 2H), 2.76 (dd, 1H), 2.52 (m, 3H), 2.10 (m, 1H), 1.29 (s, 9H), 1.08 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093406B2
Source datasetuspto-grants-2012_01
ORD IDord-daf0706536cc499ba8b821cb6015cc02
Source noteuspto-grants-2012_01