Benzyl chloroformate → (4-Methoxy-7-phenyl-benzothiazol-2-yl)-carbamic acid benzyl ester

HRID 1063012Notes

Reaction equation

HRID 1063012 reaction equation
[NH2:1][C:2]1[S:3][C:4]2[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[CH:9][CH:8]=[C:7]([O:17][CH3:18])[C:5]=2[N:6]=1.Cl[C:20]([O:22][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1)=[O:21]>N1C=CC=CC=1>[CH2:23]([O:22][C:20](=[O:21])[NH:1][C:2]1[S:3][C:4]2[C:10]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)=[CH:9][CH:8]=[C:7]([O:17][CH3:18])[C:5]=2[N:6]=1)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1

Participants

4

Procedure

To a stirred solution of 2-amino-4-methoxy-7-phenyl-benzothiazole (512 mg, 2 mmol) in pyridine at 90° C. was added benzyl chloroformate (3.3 ml, 23.4 mmol) in three portions over 6 hours. The reaction mixture was then evaporated to dryness and partioned between CH2Cl2 (50 ml) and saturated aqueous NaCl solution (50 ml), the aqueous phase was separated and extracted further with CH2Cl2 (2×50 ml) and the combined organic phases dried, filtered and evaporated. The crude residue was then chromatographed over SiO2 (Merck 230-400 mesh) eluting with CH2Cl2/EtOAc (4:1) to afford the title compound as a white foam (620 mg, 79% yield), MS: m/e=391.2 (M+H+).

Workup

  1. customThe reaction mixture was then evaporated to dryness
  2. customthe aqueous phase was separated
  3. extractionextracted further with CH2Cl2 (2×50 ml)
  4. customthe combined organic phases dried
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude residue was then chromatographed over SiO2 (Merck 230-400 mesh)
  8. washeluting with CH2Cl2/EtOAc (4:1)

Sources & evidence

ORD record
ord-b7f021de0d3641b3885d9a3d4926e9a8
Source dataset
uspto-grants-2005_11
Patent number
US06963000B2

Reaction notes

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