Aluminium lithium hydride → HCID 21341515, compound
Reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].COCN[C:11](=[O:29])[C@@H:12]([CH2:21][CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)[NH:13][C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15]>O1CCCC1>[C:14]([NH:13][C@@H:12]([CH:11]=[O:29])[CH2:21][CH2:22][C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1)([O:16][C:17]([CH3:18])([CH3:20])[CH3:19])=[O:15]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -35 °C
Procedure
A cold (−40° C.) solution of lithium aluminum hydride (25.2 mL of a 1M solution) in tetrahydrofiran (165 mL), under nitrogen, is treated with a solution of N-Boc-D-homophenylalanine methoxymethylamide (6.76 g) in tetrahydrofuran (20 mL) at such a rate as to keep the temperature between −36 to −38° C. After the addition, the temperature is allowed to rise to 7° C. after which the reaction mixture is cooled to −35° C. The mixture is quenched with 2.75 M KHSO4 solution and the mixture is stirred for 1 h while warming to 25 ° C. The aqueous layer is separated and extracted thrice with ether. The combined organics are washed successively thrice with 10% citric acid, water, saturated bicarbonate and brine, dried (MgSO4) and concentrated. The viscous clear residue solidifies under vacuum to give the title compound (5.32 g): 1H NMR (400 MHz, CDCl3) δ1.47 (s, 9H), 1.88 (m, 1H), 2.22 (m, 1H), 2.71 (t, J=7.6 Hz, 2H), 4.24 (m, 1H), 5.18 (bd, 1H, NH), 7.20 (m, 3H), 7.27 (m, 2H), and 9.54 (s, 1H).
Workup
- custombetween −36 to −38° C
- additionAfter the addition
- customto rise to 7° C.
- customThe mixture is quenched with 2.75 M KHSO4 solution
- temperaturewhile warming to 25 ° C
- customThe aqueous layer is separated
- extractionextracted thrice with ether
- washThe combined organics are washed successively thrice with 10% citric acid, water, saturated bicarbonate and brine
- dry with materialdried (MgSO4)
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-70f1e854008d46b58cbe5aacf97688d7
- Source dataset
- uspto-grants-2001_03
- Patent number
- US06204279B1
Reaction notes
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