3-Tetradecylthioacetylamino-2-tetradecylthioacetylthio-1-triphenylmethyloxypropane → 3-Tetradecylthioacetylamino-2-tetradecylthioacetylthiopropan-1-ol
Reaction equation
[CH2:1]([CH2:15][C:16]([NH:18][CH2:19][CH2:20][CH:21]([S:42][C:43](=[S:59])[CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH2:51][CH2:52][CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH3:58])[O:22]C(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)=[S:17])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]>CCOCC.Cl>[CH2:1]([CH2:15][C:16]([NH:18][CH2:19][CH2:20][CH:21]([S:42][C:43](=[S:59])[CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH2:51][CH2:52][CH2:53][CH2:54][CH2:55][CH2:56][CH2:57][CH3:58])[OH:22])=[S:17])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14]Participants
4
Procedure
3-tetradecylthioacetylamino-2-tetradecylthioacetylthio-1-triphenylmethyloxy-propane (example 20d) (187 mg, 0.21 mmol) was dissolved in ether saturated with gaseous hydrochloric acid (12 ml). The reaction medium was stirred at room temperature for 20 hours. The precipitate which formed was filtered and washed with diethyl ether to give the desired compound in the form of a white powder.
Workup
- customThe precipitate which formed
- filtrationwas filtered
- washwashed with diethyl ether
Sources & evidence
- ORD record
- ord-58f0c66fbea140fea729ec4cd5f0685c
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07253296B2
Reaction notes
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