3-Amino-1,1,1-trifluoro-3-phenylpropan-2-ol hydrochloride → HCID 59536896, compound

HRID 2402842Notes

Reaction equation

HRID 2402842 reaction equation
C(=O)(OCCC(N[C:15](=[O:37])[CH2:16][N:17]1[C:21](=[O:22])[N:20]([CH2:23][C@H:24]([OH:29])[C:25]([F:28])([F:27])[F:26])[C:19]([C:30]2[CH:35]=[CH:34][C:33]([Cl:36])=[CH:32][CH:31]=2)=[N:18]1)C1C=CC=CC=1F)N.Cl.[NH2:40][CH:41]([C:48]1[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=1)[CH:42]([OH:47])[C:43]([F:46])([F:45])[F:44]>>[Cl:36][C:33]1[CH:34]=[CH:35][C:30]([C:19]2[N:20]([CH2:23][C@H:24]([OH:29])[C:25]([F:27])([F:26])[F:28])[C:21](=[O:22])[N:17]([CH2:16][C:15]([NH:40][CH:41]([C:48]3[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=3)[CH:42]([OH:47])[C:43]([F:44])([F:45])[F:46])=[O:37])[N:18]=2)=[CH:31][CH:32]=1

Participants

3

Procedure

In the same way as for the compound from Example 93, 100 mg (0.27 mmol) of the compound from Example 8A and 73 mg (0.30 mmol) of 3-amino-1,1,1-trifluoro-3-phenylpropan-2-ol hydrochloride were reacted. This gave 102 mg (63% of theory) of the target compound as a diastereomer mixture.

Sources & evidence

ORD record
ord-ad1cb1fa5b024128b9ec55627952eb31
Source dataset
uspto-grants-2014_08
Patent number
US08796324B2

Reaction notes

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