Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 86685932 | HCID 86685932 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86685933 | HCID 86685933 | 116.3% |
Reaction Steps
Thionyl chloride (1.4 mL, 19.0 mmol) was added slowly at 0° C. to a solution of 5-chloro-2-(5-hydroxymethyl-pyridin-3-yl)-3,3-dimethyl-2,3-dihydro-isoindol-1-one (1.14 g, 3.8 mmol) in DCM (50 mL). After the addition, the reaction mixture was stirred at 2-5° C. for 2 hours before it was poured into satd. aq. NaHCO3 solution (50 mL) and extracted with EtOAc (2×150 mL). The organic layer was washed with brine, dried over anhy. Na2SO4, filtered and concentrated in vacuo to give a crude product (1.42 g, 92%) as a light yellowish solid. MS: 322.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133158B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-6f1a562041ad4e859794601b91cba4cd |
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| Source note | uspto-grants-2015_09 |
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