Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 19025627 | HCID 19025627 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 19025652 | HCID 19025652 | — |
Reaction Steps
A mixture of 0.5 g of 3-iodo-7-methylthio-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one and 15 g of ammonia in 20 mL of chloroform was shaken in a bomb at 100° C. for 3 hours. The bomb was cooled, vented and the contents transferred to a separatory funnel. The mixture was washed with water, dried over magnesium sulfate, filtered and solvents removed under vacuum to give the product. 1H NMR (200 MHz, CDCl3): 1.90 (m,1H), 2.3-2.7 (m,2H), 2.45 (s,3H), 2.85 (m,1H), 3.39 (dd;8,11 Hz;1H), 6.89 (d,8 Hz,1H), 7.10 (m,2H), 8.3 (br s,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05206235 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-98bdd6b05ef94ef8afcbcb5d1dfea6fd |
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| Source note | uspto-grants-1993_04 |
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