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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510320Generated: October 30, 2026

Sodium Hydroxide → HCID 86699851, compound

https://huagongshe.com/reaction/510320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86699852HCID 86699852—
SolventMethanolHCID 887—
ProductHCID 86699851HCID 86699851—

Reaction Steps

To a solution of (2S)-methyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(3-phenylpyrrolidin-1-yl)benzo[d]thiazol-6-yl)acetate (29.3 mg, 0.653 mmol) in CH3OH (1 mL) was added NaOH (1N, 1 mL, 1 mmol), the resulting mixture was heated at 50 C for 10 hr. The mixture was acidified to pH 3 and evaporated to a small volume, and the residue was partitioned between CH2Cl2 and brine. The organic layer was separated, dried, filtered and evaporated to dryness. The residue was purified on TLC (50% EtOAc/Hex) to give (2S)-2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(3-phenoxypyrrolidin-1-yl)benzo[d]thiazol-6-yl)acetic acid. LCMS-ESI+: calc'd for C30H32ClN2O3S: 534.2, 536.2 (M+H+); found: 535.2, 537.2 (M+H+). 1H-NMR: 400 MHz, (CD3OD) δ: 7.63 (dd, J=2.0, 7.2 Hz, 1H), 7.49-7.52 (m, 3H), 7.30-7.34 (m, 5H), 7.24 (m, 1H), 5.13 (s, 1H), 3.94 (m, 1H), 3.70 (m, 1H), 3.52-3.63 (m, 4H), 2.48 (s, 3H), 2.46 (m, 1H), 2.20 (m, 1H), 0.94 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096586B2
Source datasetuspto-grants-2015_08
ORD IDord-6430e184bc824cd49424bef4171d299a
Source noteuspto-grants-2015_08