Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1-Chloro-N,N-2-trimethylpropenylamine | HCID 640792 | — |
| Reactant | tert-Butyl 3-amino-1H-pyrazole-1-carboxylate | HCID 51358380 | — |
| Reactant | 3-[(1,1-dioxido-3,4-dihydro-2H-5,1,2-benzoxathiazepin-7-yl)oxy]-5-{[(S)-1-methyl-2-(methyloxy)ethyl]oxy}benzoic acid | HCID 57663222 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57663157 | HCID 57663157 | 16% |
Reaction Steps
1-Chloro-N,N,2-trimethyl-1-propenylamine (0.1 mL, 0.74 mmol) was added to a solution of 3-[(1,1-dioxido-3,4-dihydro-2H-5,1,2-benzoxathiazepin-7-yl)oxy]-5-{[(S)-1-methyl-2-(methyloxy)ethyl]oxy}benzoic acid (0.21 g, 0.50 mmol) in DCM (5 mL) and stirred for 1 hour. 1,1-Dimethylethyl 3-amino-1H-pyrazole-1-carboxylate (137 mg, 0.74 mmol) then pyridine (0.08 mL, 0.99 mmol) were added and the reaction stirred for a further 45 minutes. The mixture was reduced in vacuo and ethyl acetate (50 mL) and water (50 mL) added. The aqueous layer was re-extracted into ethyl acetate (50 mL) and the combined organics washed with water (50 mL), brine (50 mL), dried (MgSO4), filtered and reduced in vacuo to give a golden oil which was chromatographed on silica, eluting with 30-60% ethyl acetate in isohexane, to give a colourless oil. The oil was dissolved in ethyl acetate (30 mL) and washed with 1M hydrochloric acid, dried (MgSO4), filtered and reduced in vacuo to give the desired compound as a colourless oil (47 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943607B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-c7bae9d0be03412ca40e2291f6a90484 |
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| Source note | uspto-grants-2011_05 |
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