Ammonia → HCID 53881535, compound
Reaction equation
[C:1]1([CH2:7][O:8][C:9]2[CH:17]=[CH:16][C:15]3[N:14]([CH3:18])[C:13]4[CH2:19][CH:20]([C:22]([OH:24])=O)[CH2:21][C:12]=4[C:11]=3[CH:10]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH3:25]>C(O)C>[C:1]1([CH2:7][O:8][C:9]2[CH:17]=[CH:16][C:15]3[N:14]([CH3:18])[C:13]4[CH2:19][CH:20]([C:22]([NH2:25])=[O:24])[CH2:21][C:12]=4[C:11]=3[CH:10]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
In a sealed tube was added a solution of 1,2,3,4-tetrahydro-7-phenylmethoxy-4-methylcyclopent[b]indole-2-carboxylic acid ecid ethyl ester (5.0 g, 0.014 mole) in 25 ml of absolute ethanol, followed by ammonia (30% aqueous solution, 10ml, 0.17 mole). After heating at 100° C. for five days, the mixture was cooled and the resultant tan precipitate collected and dried to give 3.0 g, m.p. 145°-148° C.
Workup
- temperaturethe mixture was cooled
- customthe resultant tan precipitate collected
- customdried
- customto give 3.0 g, m.p. 145°-148° C.
Sources & evidence
- ORD record
- ord-0facbd66cb9a4fa7b97227148a70c0d1
- Source dataset
- uspto-grants-1994_09
- Patent number
- US05350762
Reaction notes
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