Methylamine hydrochloride → HCID 90449316, compound

HRID 1411290Notes

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]([O:17][CH2:18][CH2:19][CH2:20][C:21](O)=[O:22])[CH:15]=3)[N:10]([C:24](=[O:32])[NH:25][C:26]3[S:27][C:28]([Cl:31])=[CH:29][N:30]=3)[CH2:9]2)[CH2:5]1)(=[O:3])[CH3:2].Cl.[CH3:34][NH2:35]>>[C:1]([N:4]1[CH2:8][CH2:7][C:6]2([C:16]3[C:11](=[CH:12][CH:13]=[C:14]([O:17][CH2:18][CH2:19][CH2:20][C:21]([NH:35][CH3:34])=[O:22])[CH:15]=3)[N:10]([C:24]([NH:25][C:26]3[S:27][C:28]([Cl:31])=[CH:29][N:30]=3)=[O:32])[CH2:9]2)[CH2:5]1)(=[O:3])[CH3:2]

Participants

Reactant 2

HCID 6364545Methylamine hydrochloride

HCID 90449610HCID 90449610, compound

Product 1

HCID 90449316HCID 90449316, compound

Procedure

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

Sources & evidence

ORD record: ord-fd1d1fe5d52b47d1a623196aefbab451
Source dataset: uspto-grants-2014_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08921576B2

Reaction notes

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