NADPH → HCID 70655394, compound

HRID 1972396Notes

Reaction equation

HRID 1972396 reaction equation
[F:1][C:2]([F:35])([F:34])[C@@:3]([C:6]1[CH:11]=[CH:10][C:9]([N:12]2[CH2:17][CH2:16][N:15]([S:18]([C:21]3[S:22][CH:23]=[CH:24][CH:25]=3)(=[O:20])=[O:19])[CH2:14][C@@H:13]2[CH2:26][C:27]2[CH:32]=[CH:31][CH:30]=[C:29]([F:33])[CH:28]=2)=[CH:8][CH:7]=1)([OH:5])[CH3:4].FC(F)(F)[C@](C1C=CC(N2CCN(S(C3SC=CC=3)(=O)=O)C[C@H]2CC2C=CC=C(F)C=2)=CC=1)(O)C.FC(F)(F)[C@](C1C=CC(N2CCN(S(C3SC=CC=3)(=O)=O)C[C@@H]2CC2C=CC=C(F)C=2)=CC=1)(O)C.C1N=C(N)C2N=CN([C@@H]3O[C@H](COP(OP(OC[C@H]4O[C@@H](N5C=C(C(N)=O)CC=C5)[C@H](O)[C@@H]4O)(O)=O)(O)=O)[C@@H](O)[C@H]3OP(O)(O)=O)C=2N=1>>[F:35][C:2]([F:1])([F:34])[C@@:3]([C:6]1[CH:11]=[CH:10][C:9]([N:12]2[CH2:17][CH2:16][N:15]([S:18]([C:21]3[S:22][CH:23]=[CH:24][CH:25]=3)(=[O:20])=[O:19])[CH2:14][C@H:13]2[CH2:26][C:27]2[CH:32]=[CH:31][CH:30]=[C:29]([F:33])[CH:28]=2)=[CH:8][CH:7]=1)([OH:5])[CH3:4]

Participants

5

Reactant 4

HCID 5884NADPHHCID 66586134HCID 66586134, compoundHCID 66586180HCID 66586180, compoundHCID 70655755HCID 70655755, compound

Product 1

HCID 70655394HCID 70655394, compound

Procedure

(2R)-1,1,1-trifluoro-2-(4-((2S)-2-(3-fluorobenzyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-2-propanol; (2S)-1,1,1-trifluoro-2-(4-((2R)-2-(3-fluorobenzyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-2-propanol; (2S)-1,1,1-trifluoro-2-(4-((2S)-2-(3-fluorobenzyl)-4-(2-thiophenylsulfonyl)-1-piperazinyl)phenyl)-2-propanol. 1H NMR (400 MHz, CD3OD) δ 7.86 (dd, J=1.2, 5.1 Hz, 1H), 7.64-7.59 (m, 1H), 7.55-7.48 (m, 2H), 7.36-7.15 (m, 2H), 7.11-6.77 (m, 5H), 4.17-4.09 (m, 1H), 3.84 (d, J=10.0 Hz, 1H), 3.61 (d, J=11.3 Hz, 1H), 3.55-3.43 (m, 1H), 3.42-3.34 (m, 1H), 3.19-3.04 (m, 1H), 2.69-2.48 (m, 3H), 1.70 (s, 3H). m/z (ESI, +ve ion) 529.0 (M+H)+. GK-GKRP EC50 (NADPH-coupled)=0.802 μM; GK-GKRP EC50 (LC MS/MS)=1.09 μM.

Sources & evidence

ORD record
ord-91bd9006d38343b489c1c75163698777
Source dataset
uspto-grants-2013_04
Patent number
US08431563B2

Reaction notes

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