Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 178453655 | HCID 178453655 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178453662 | HCID 178453662 | 85% |
Reaction Steps
Inter-mediate 10, tert-butyl [(cis-3-hydroxycyclobutyl)methyl]carbamate (3 g, 15 mmol) and triethylamine (5.2 mL, 36 mmol) were dissolved in CH2Cl2 (50 mL). MsCl (1.4 mL, 18 mmol) was added dropwise under stirring and cooling with an ice bath in argon. The temperature was brought to ambient within 1 h. Water (50 mL) was added, and the layers were separated. The organic one was washed with water, brine, dried with Na2SO4, and evaporated. The title compound (3.5 g, 85%) was obtained as a yellow oil. This crude product was used for the next stage without additional purification. 1H NMR-data (DMSO-d6): 6.74-7.00 (m, 1H, NH); 4.73-4.86 (m, 1H); 3.10 (s, 3H, MS); 2.97 (t, 2H, CH2, J=5.7 Hz); 2.32-2.42 (m, 2H); 1.80-2.43 (m, 3H); 1.38 (s, 9H, Boc).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812040B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-b21f814cffd24f33ba1404544d4be7b0 |
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| Source note | uspto-grants-2010_10 |
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