Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 53378258 | HCID 53378258 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 71082614 | HCID 71082614 | 170.4% |
Reaction Steps
65 mg of (S)-methyl 2-(2-(2,2-dimethylbutanoyloxy)-6,7-dihydrothieno[3,2-c]pyridin-5(4H)-yl)-2-(2-chlorophenyl)-acetate (I-8) was dissolved in 4 ml of diethyl ether, and stirred in an ice-salt bath at −10° C. A hydrogen chloride saturated ethanol solution (0.2 ml) was added slowly dropwise, till the system reached about pH 2, at which a white solid was precipitated immediately. It was stirred for 5 min, then allowed to stand, quickly filtered under a nitrogen atmosphere, and washed with a suitable amount of diethyl ether. The resulting solid was dried in vacuum to obtain the I-8 hydrochloride (60 mg, white granular solid). Yield: 88%, melting point: 133-135° C.; 1H-NMR (300 MHz, CDCl3) δ 0.91 (t, 3H, J=7.6 Hz), 1.29 (s, 6H), 1.69 (q, 2H, J=7.4 Hz), 3.08 (s, 1H), 3.48 (m, 2H), 3.83 (s, 4H), 4.35 (s, 1H), 5.59 (s, 1H), 6.37 (s, 1H), 7.44-7.50 (m, 3H), 8.36 (d, 1H, J=6.84 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772489B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-41dd4c43d787440fbd87b5b898fae79c |
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| Source note | uspto-grants-2014_07 |
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