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

HRID 2250722Notes

Reaction equation

HRID 2250722 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 CH2Cl2EtOAc (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 CH2Cl2EtOAc (4:1)

Sources & evidence

ORD record
ord-e5023c21862d4ad2aa0941c23b2ad6c9
Source dataset
uspto-grants-2008_01
Patent number
US07317007B2

Reaction notes

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