Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 12507637 | HCID 12507637 | — |
| Product | HCID 12800954 | HCID 12800954 | — |
Reaction Steps
A suspension of 4,5-dihydro-3-(1,3,4,9-tetrahydro-1-methyl pyrano[3,4-b]indol-1-yl]-2(3H)-furanone (described in Example 1, 20 g, 0.073 mole) in liquid ammonia is heated at 90° C. in a pressure apparatus for three hours. The apparatus is rinsed with ethanol and the yellow solution is evaporated. The residue is crystallized from ethanol to afford α-(2-hydroxyethyl)-1-methyl-1,3,4,9-tetrahydropyrano[ 3,4-b]-indole-1-acetamide (16.15 g) , m.p. 159°-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04179503 |
|---|
| Source dataset | uspto-grants-1979_12 |
|---|
| ORD ID | ord-c1f0481a9b844001be66000fbc1cbff9 |
|---|
| Source note | uspto-grants-1979_12 |
|---|