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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094316Generated: November 2, 2026

Bromopinacolone → HCID 86645971, compound

https://huagongshe.com/reaction/1094316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromopinacoloneHCID 21642—
ReactantHCID 86645968HCID 86645968—
ReactantHCID 86645970HCID 86645970—
ProductHCID 86645971HCID 8664597155%

Reaction Steps

The acid was obtained following the same procedure described for (2R)-2-(4-{[4-(trifluoromethyl)-1,3-thiazol-2-yl]amino}phenyl)propanoic acid and starting from methyl (2R)-2-[4-(carbamothioylamino)phenyl]propanoate (2.0 g, 8.40 mmol) and 1-bromopinacolone (1.13 ml, 8.40 mmol). The following acid hydrolysis afforded the pure (2R)-2-{4-[(4-tert-butyl-1,3-thiazol-2-yl)amino]phenyl}propanoic acid (1.41 g, 4.62 mmol) as pale yellow oil (55%). 1H-NMR (CDCl3): δ 8.30 (bs, 1H, NH), 7.40 (d, 2H, J=7 Hz), 7.20 (d, 2H, J=7 Hz), 6.40 (s, 1H), 3.75 (q, 1H, J=7 Hz), 1.50 (d, 3H, J=7 Hz), 1.40, (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08133911B2
Source datasetuspto-grants-2012_03
ORD IDord-652427ad59df46b29b7457b84c5f6445
Source noteuspto-grants-2012_03