Azetidine hydrochloride → HCID 90449822, compound

HRID 1411292Notes

Reaction equation

[C:1]([N:4]1[CH2:8][CH2:7][C:6]2([C:16]3[C:11](=[CH:12][CH:13]=[C:14]([CH2:17][CH2:18][CH2:19][C:20]([OH:22])=O)[CH:15]=3)[N:10]([C:23](=[O:31])[NH:24][C:25]3[S:26][C:27]([Cl:30])=[CH:28][N:29]=3)[CH2:9]2)[CH2:5]1)(=[O:3])[CH3:2].Cl.[NH:33]1[CH2:36][CH2:35][CH2:34]1>>[C:1]([N:4]1[CH2:8][CH2:7][C:6]2([C:16]3[C:11](=[CH:12][CH:13]=[C:14]([CH2:17][CH2:18][CH2:19][C:20]([N:33]4[CH2:36][CH2:35][CH2:34]4)=[O:22])[CH:15]=3)[N:10]([C:23]([NH:24][C:25]3[S:26][C:27]([Cl:30])=[CH:28][N:29]=3)=[O:31])[CH2:9]2)[CH2:5]1)(=[O:3])[CH3:2]

Participants

Reactant 2

HCID 12308726Azetidine hydrochloride

HCID 90449676HCID 90449676, compound

Product 1

HCID 90449822HCID 90449822, compound

Procedure

4-(1′-Acetyl-1-((5-chlorothiazol-2-yl)carbamoyl)spiro[indoline-3,3′-pyrrolidin]-5-yl)butanoic acid and azetidine hydrochloride

Sources & evidence

ORD record: ord-73ee6421a63b407ca7f8c044e55f57f4
Source dataset: uspto-grants-2014_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08921576B2

Reaction notes

Loading…