Isopropyl isocyanate → HCID 23367272, compound

HRID 1080419Notes

Reaction equation

HRID 1080419 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]=1

Participants

6

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

  1. filtrationThe reaction was filtered through neutral alumina eluting with EtOAc (3 l)
  2. concentrationthe filtrate was concentrated in vacuo
  3. 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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