Benzhydrylamine → HCID 86680446, compound
Reaction equation
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][N:11]2[CH2:14][C@@H:15]([C:17]([OH:19])=O)[CH2:16][C@H:10]2[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C(N=C=NCCCN(C)C)C.O.OC1C2N=NNC=2C=CC=1.[C:42]1([CH:48]([C:50]2[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=2)[NH2:49])[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1>ClCCl.O>[CH:48]([NH:49][C:17]([C@@H:15]1[CH2:14][N:11]2[CH2:12][CH2:13][N:8]([C:6]([O:5][C:1]([CH3:2])([CH3:3])[CH3:4])=[O:7])[CH2:9][C@@H:10]2[CH2:16]1)=[O:19])([C:50]1[CH:51]=[CH:52][CH:53]=[CH:54][CH:55]=1)[C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of (7S,8aS)-2-(tert-butoxycarbonyl)octahydropyrrolo[1,2-a]pyrazine-7-carboxylic acid (80 mg, 0.296 mmol) in dichloromethane (2 mL) was added a solution of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (68.9 mg, 0.444 mmol) and hydroxybenzotriazole hydrate (40.0 mg, 0.296 mmol) in dichloromethane (1 mL). The mixture was stirred at room temperature for 1 hour and then diphenylmethanamine (54.2 mg, 0.296 mmol) was added. After stirring for three days the mixture was poured into water (10 mL). The mixture was extracted with dichloromethane (3×5 mL), the organic fractions were concentrated and the residue was purified by flash chromatography (dichloromethane/methanol=25:1) to give the title compound. MS (ESI) m/z 436 (M+H)+.
Workup
- stirringAfter stirring for three days the mixture
- extractionThe mixture was extracted with dichloromethane (3×5 mL)
- concentrationthe organic fractions were concentrated
- customthe residue was purified by flash chromatography (dichloromethane/methanol=25:1)
Sources & evidence
- ORD record
- ord-f2097449085248e596fd89dcd36a5cb5
- Source dataset
- uspto-grants-2014_03
- Patent number
- US08669255B2
Reaction notes
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