4,4-Difluoropiperidine hydrochloride → (S)-2'-(4,4-difluoropiperidin-1-yl)-4'-fluoro-7'-(2-fluoropyridin-3-yl)-5H-spiro[thiazole-4,9'-xanthen]-2-amine

HRID 336020Notes

Reaction equation

HRID 336020 reaction equation
[NH2:1][C:2]1[S:3][CH2:4][C@@:5]2([N:22]=1)[C:18]1[CH:17]=[C:16](O)[CH:15]=[C:14]([F:20])[C:13]=1[O:12][C:11]1[C:6]2=[CH:7][C:8](Br)=[CH:9][CH:10]=1.[F:23][C:24]1[C:29](B(O)O)=[CH:28][CH:27]=[CH:26][N:25]=1.Cl.[F:34][C:35]1([F:41])[CH2:40][CH2:39][NH:38][CH2:37][CH2:36]1>>[F:34][C:35]1([F:41])[CH2:40][CH2:39][N:38]([C:16]2[CH:15]=[C:14]([F:20])[C:13]3[O:12][C:11]4[C:6](=[CH:7][C:8]([C:29]5[C:24]([F:23])=[N:25][CH:26]=[CH:27][CH:28]=5)=[CH:9][CH:10]=4)[C@@:5]4([CH2:4][S:3][C:2]([NH2:1])=[N:22]4)[C:18]=3[CH:17]=2)[CH2:37][CH2:36]1

Participants

4

Procedure

The titled compound was synthesized by stpes analogous to those described in method AA20 above, but using (S)-2-amino-7′-bromo-4′-fluoro-5H-spiro[thiazole-4,9′-xanthen]-2′-ol (prepared as described in Method BB26 and Example 2 but using 7-bromo-4-fluoro-2-methoxy-9H-xanthen-9-one), 2-fluoropyridin-3-ylboronic acid and 4,4-difluoropiperidine hydrochloride. MS m/z=501.0.0 [M+H]+.

Sources & evidence

ORD record
ord-737428b6fb1c48239fe75b06900d6372
Source dataset
uspto-grants-2014_11
Patent number
US08883782B2

Reaction notes

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