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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103725Generated: October 31, 2026

Water → HCID 178461179, compound

https://huagongshe.com/reaction/2103725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178497325HCID 178497325—
SolventMethanolHCID 887—
ProductHCID 178461179HCID 178461179111.1%

Reaction Conditions

Temperature23 °C

Reaction Steps

Methyl 2-{trans-3-[(S)-2-methylpiperidin-1-yl]cyclobutyl}-1,3-benzothiazole-6-carboxylate (Example 143A, 2.0 g, 5.8 mmol) was dissolved in methanol (600 mL), followed by H2O (300 mg, 16.7 mmol) and sodium methoxide (1.4 g, 26 mmol) at 23° C. The reaction mixture was then allowed to stir at 23° C. for 1 day. Solvent and excess of water were removed. HCl (2N) was added to make the mixture slightly acidic (pH ˜5-6). Excess of water was removed. The solid was triturated with CH2Cl2/MeOH, and filtrated. The solvents of the filtrate were removed under vacuum. The residue was treated with CH2Cl2 and filtrated again. Removal of the solvent gave the desired product as an off-white solid (2.13 g, 100%). 1H NMR (300 MHz, CD3OD): δ=8.54 ppm (d, J=1.3 Hz, 1H), 8.11 (dd, J=8.9, 1.3 Hz, 1H), 7.91 (d, J=8.9 Hz, 1H), 4.00 (m, 1H), 3.80 (m, 1H), 2.70-3.10 (m, 7H), 2.00 (m, 2H), 1.80 (m, 2H), 1.65 (m, 2H), 1.41 (d, J=6.8 Hz, 3H). MS (ESI, M+H+): 331.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576110B2
Source datasetuspto-grants-2009_08
ORD IDord-11cac81a62884741b1704dd1ab2a15d7
Source noteuspto-grants-2009_08