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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420312Generated: October 31, 2026

Chloroacetyl chloride → HCID 131729386, compound

https://huagongshe.com/reaction/420312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantHCID 66649644HCID 66649644—
SolventTolueneHCID 1140—
ProductHCID 131729386HCID 131729386—

Reaction Steps

The title compound was prepared in analogous manner as described for example 8p) from (3aR,7S,7aS)-7-[4-amino-3-fluoro-5-(2,2,2-trifluoro-ethoxy)-benzyl]-3-(3-tert-butyl-benzyl)-5,5-dioxo-hexahydro-1-oxa-5lambda*6*-thia-3-aza-inden-2-one (400 mg, 0.716 mmol) and chloroacetylchloride (324 mg, 2.86 mmol) to yield a white foam: TLC Rf=0.40 (toluene-ETA 85:15); ESIMS [M+NH4]+=652, 654, [M−H]−=633, 635; UPLC RtD=1.861 min; 1H NMR (600 MHz, DMSO-d6): δ 9.64 (s, 1H, NH), 7.41 (s, 1H), 7.33 (d, 1H), 7.28 (t, 1H), 7.13 (d, 1H), 6.91 (s, 1H), 6.88 (d, 1H), 4.74 (q, 2H), 4.43 (d, 1H), 4.25-4.18 (m, 4H), 3.78 (d, 1H), 3.65 (t, 1H), 3.50 (t, 1H), 3.17 (t, 1H), 2.99 (m, 2H), 2.56 (m, 2H), 1.25 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093406B2
Source datasetuspto-grants-2012_01
ORD IDord-8f87e8c24ef94e74b683786f56286aa6
Source noteuspto-grants-2012_01