Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | HCID 67398866 | HCID 67398866 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66746870 | HCID 66746870 | 52% |
Reaction Steps
To a solution of chlorosulfonyl isocyanate (212 mg, 1.50 mmol) in CH2Cl2 (0.55 mL) at 0° C., was added formic acid (0.575 mL) under N2. The reaction was stirred for 30 min, and a solution of 2-amino-6-(4-methoxybenzyloxy)benzonitrile (Example 114b) (191 mg, 0.75 mmol) in CH2Cl2 (4 mL) was added at 0° C., followed by Et3N (0.627 mL, 4.50 mmol). After 30 min, the reaction was concentrated in vacuo and diluted with water. The pH was adjusted to 7 with concentrated HCl, and purified by reverse phase HPLC (10-90% acetonitrile in water) to provide 2-sulfamoylamino-6-(4-methoxybenzyloxy)benzonitrile (130 mg, 52%). 1H NMR (400 MHz, MeOD) δ 3.80 (s, 3H), 5.15 (s, 2H), 6.88 (d, J=8.1 Hz 1H), 6.94 (m, 2H), 7.40 (m, 2H), 7.48 (t, J=8.7 Hz, 1H), 7.75 (dd, J=8.6, 0.8 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633186B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-80fcf54f0ba74971a903f865025da67f |
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| Source note | uspto-grants-2014_01 |
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