Isopropyl isocyanate → HCID 23367272, compound
Reaction equation
[N:1]1([CH2:7][CH2:8][N:9]([CH3:20])[C:10]2[C:14]3[CH:15]=[CH:16][C:17]([OH:19])=[CH:18][C:13]=3[O:12][N:11]=2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[CH3:21][CH:22]([N:24]=[C:25]=[O:26])C.CO.C(Cl)Cl>CCOC(C)=O.[Cu]Cl>[CH3:21][CH2:22][NH:24][C:25](=[O:26])[O:19][C:17]1[CH:16]=[CH:15][C:14]2[C:10]([N:9]([CH2:8][CH2:7][N:1]3[CH2:6][CH2:5][O:4][CH2:3][CH2:2]3)[CH3:20])=[N:11][O:12][C:13]=2[CH:18]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
To a stirred solution of 3-[[2-(4-morpholinyl)ethyl]methylamino]-1,2-benzisoxazol-6-ol (2.2 g) and copper(I)chloride (0.1 g) in EtOAc (50 ml) was added 1-methylethylisocyanate (0.8 g). After 24 hours TLC (silica gel, 10% MeOH/DCM) showed no starting material. The reaction was filtered through neutral alumina eluting with EtOAc (3 l) and the filtrate was concentrated in vacuo. The white solid was flash chromatographed on silica gel eluting with 1% MeOH/DCM to yield 1.2 g of the product, m.p. 99°-100° C.
Workup
- filtrationThe reaction was filtered through neutral alumina eluting with EtOAc (3 l)
- concentrationthe filtrate was concentrated in vacuo
- customchromatographed on silica gel eluting with 1% MeOH/DCM
Sources & evidence
- ORD record
- ord-19ebbbe41e5d4c2696b2d14fbe35cab7
- Source dataset
- uspto-grants-1996_12
- Patent number
- US05580982
Reaction notes
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