Silica → HCID 58625068, compound

HRID 2088806Notes

Reaction equation

HRID 2088806 reaction equation
[C:1]([O:5][C:6](=[O:39])[NH:7][C:8]1[N:17]([CH2:18][CH2:19][CH3:20])[CH2:16][C:15]2[C:10](=[CH:11][CH:12]=[C:13]([O:21][C:22]3[CH:27]=[CH:26][CH:25]=[C:24]([NH:28]C(OCC4C=CC=CC=4)=O)[CH:23]=3)[CH:14]=2)[N:9]=1)([CH3:4])([CH3:3])[CH3:2].O=[Si]=O>CO.[Pd]>[C:1]([O:5][C:6](=[O:39])[NH:7][C:8]1[N:17]([CH2:18][CH2:19][CH3:20])[CH2:16][C:15]2[C:10](=[CH:11][CH:12]=[C:13]([O:21][C:22]3[CH:27]=[CH:26][CH:25]=[C:24]([NH2:28])[CH:23]=3)[CH:14]=2)[N:9]=1)([CH3:2])([CH3:3])[CH3:4]

Participants

5

Procedure

A mixture of [6-(3-benzyloxycarbonylamino-phenoxy)-3-propyl-3,4-dihydro-quinazolin-2-yl]-carbamic acid tert-butyl ester (0.008 mol) in methanol (150 mL) was hydrogenated with 10% Pd/C (1 g) as a catalyst. After uptake of H2 gas (1 equiv.), the reaction mixture was filtered over Dicalite and the filtrate was evaporated. The residue was stirred in diisopropyl ether and the resulting precipitate was filtered off and dried to yield the title compound as a solid.

Workup

  1. customthe filtrate was evaporated
  2. filtrationthe resulting precipitate was filtered off
  3. customdried

Sources & evidence

ORD record
ord-4b4927bbb4024b95af5d8766b95663a0
Source dataset
uspto-grants-2013_05
Patent number
US08436006B2

Reaction notes

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